NOVEL a4B7 PEPTIDE MONOMER AND DIMER ANTAGONISTS

ABSTRACT

The invention relates to peptide dimer compounds and peptide monomer compounds that potently inhibit binding of α4β7 to the mucosal addressin cell adhesion molecule (MAdCAM) in vivo, possess high selectivity against α4β1 binding, and have high stability under gastrointestinal conditions.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Continuation of U.S. application Ser. No. 15/698,407, filed Sep. 7, 2017, which is a Continuation of U.S. application Ser. No. 14/872,975, filed Oct. 1, 2015, now U.S. Pat. No. 9,809,623, issued Nov. 7, 2017; which claims priority to U.S. Provisional Application No. 62/058,506, filed on Oct. 1, 2014; U.S. Provisional Application No. 62/058,510, filed on Oct. 1, 2014; U.S. Provisional Application No. 62/149,257, filed on Apr. 17, 2015; and U.S. Provisional Application No. 62/192,934, filed on Jul. 15, 2015; all of which are incorporated by reference herein in their entireties.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Feb. 3, 2020, is named PRTH-012-06US_SL.txt and is 173 KB in size.

FIELD OF THE INVENTION

The present invention relates to novel compounds having activity useful for treating conditions that arise from or are exacerbated by integrin binding, pharmaceutical compositions comprising the compounds, methods of treatment using the compounds, and methods of blocking or disrupting integrin binding.

BACKGROUND OF THE INVENTION

Integrins are noncovalently associated α/β heterodimeric cell surface receptors involved in numerous cellular processes ranging from cell adhesion and migration to gene regulation (Dubree, et al., Selective α4β7 Integrin Antagonist and Their Potential as Anti-inflammatory Agents, J. Med. Chem. 2002, 45, 3451-3457). Differential expression of integrins can regulate a cell's adhesive properties, allowing different leukocyte populations to be recruited to specific organs in response to different inflammatory signals. If left unchecked, integrins-mediated adhesion process can lead to chronic inflammation and autoimmune disease.

The α4 integrins, α4β1 and α4β7, play essential roles in lymphocyte migration throughout the gastrointestinal tract. They are expressed on most leukocytes, including B and T lymphocytes, where they mediate cell adhesion via binding to their respective primary ligands, vascular cell adhesion molecule (VCAM), and mucosal addressin cell adhesion molecule (MAdCAM), respectively. The proteins differ in binding specificity in that VCAM binds both α4β1 and to a lesser extent α4β7, while MAdCAM is highly specific for α4β7. In addition to pairing with the α4 subunit, the β7 subunit also forms a heterodimeric complex with αE subunit to form αEβ7, which is primarily expressed on intraepithelial lymphocytes (IEL) in the intestine, lung and genitourinary tract. αEβ7 is also expressed on dendritic cells in the gut. The αEβ7 heterodimer binds to E-cadherin on the epithelial cells. The IEL cells are thought to provide a mechanism for immune surveillance within the epithelial compartment. Therefore, blocking αEβ7 and α4β7 together may be a useful method for treating inflammatory conditions of the intestine

Inhibitors of specific integrin-ligand interactions have been shown effective as anti-inflammatory agents for the treatment of various autoimmune diseases. For example, monoclonal antibodies displaying high binding affinity for α4β7 have displayed therapeutic benefits for gastrointestinal auto-inflammatory/autoimmune diseases, such as Crohn's disease, and ulcerative colitis. Id. However, one of these therapies interfered with α4β1 integrin-ligand interactions thereby resulting in dangerous side effects to the patient. Therapies utilizing a dual-specific small molecule antagonists have shown similar side effects in animal models.

Accordingly, there is a need in the art for integrin antagonist molecules having high affinity for the α4β7 integrin and high selectivity against the α4β1 integrin, as a therapy for various gastrointestinal autoimmune diseases.

Such integrin antagonist molecules and related compositions and methods are provided by the present invention.

SUMMARY OF THE INVENTION

The present invention has been developed in response to the present state of the art, and in particular, in response to the problems and needs in the art that have not yet been fully solved by currently available integrin antagonists. Thus, the present invention provides α4β7 antagonist monomer and dimer peptides, e.g., for use as anti-inflammatory and/or immunosuppressive agents. Further, the present invention provides α4β7 antagonist monomer and dimer peptides for use in treating a condition that is associated with a biological function of α4β7 to tissues expressing MAdCAM.

The invention relates to novel peptidic compounds exhibiting integrin antagonist activity. The present invention further relates to novel peptidic compounds exhibiting high specificity for α4β7 integrin, and increased oral stability. In particular embodiments, the present invention relates to novel compounds having activity useful for treating conditions which arise or are exacerbated by integrin binding, pharmaceutical compositions comprising the compounds, methods of treatment using the compounds, and methods of blocking or disrupting integrin binding. The compounds are integrin antagonist molecules having high affinity for the α4β7 integrin, which may be used as a therapy for various gastrointestinal autoimmune diseases.

In certain embodiments, compounds of the present invention are dimers comprising two paired subunits that are linked together by their C- or N-termini via a linking moiety. In certain embodiments, one or both of the dimer subunit peptides of the present invention further comprises two natural or unnatural amino acids that are capable of bridging to form a cyclized structure. Thus, particular compounds of the present invention comprise dimerized peptides, each subunit of the dimer containing a cyclized structure through at least one of a disulfide bridge, an amide bond, or another or equivalent connection. This feature provides increased stability to the compound when administered orally as a therapeutic agent. In addition, this feature further provides for increased specificity and potency.

One having skill in the art will appreciate that the C- and N-terminal linker moieties disclosed herein are non-limiting examples of suitable linkers, and that the present invention may include any suitable linker moiety. Thus, some embodiments of the present invention comprises a homo- or heterodimer molecule comprised of two monomer subunits selected from the peptide molecules described herein and in the accompanying figures and tables, wherein the C- or N-termini of the respective monomers are linked by any suitable linker moiety to provide a dimer molecule having superior integrin antagonist activity.

In another aspect, the present invention provides a composition for treating a subject in need of integrin-antagonist therapy comprising a dimer compound of Formula (I), or any other compound described herein or in the accompanying figures and tables, in combination with a pharmaceutically acceptable carrier.

In yet another aspect, the present invention provides a diagnostic method for visualizing and diagnosing a disease comprising administering an orally stable compound of Formula (I), or any other compound described herein or in the acompanying figures, that is further labeled with at least one of a chelating group and a detectable label for use as an in vivo imaging agent for non-invasive diagnostic procedures.

In certain embodiments, compounds of the present invention are monomers. Each monomer peptide of the present invention further comprises two natural or unnatural amino acids that are capable of bridging to form a cyclized structure. Thus, the compounds of the present invention comprise monomer peptides, each forming a cyclized structure through at least one of a disulfide salt bridge, an amide bond, or an equivalent connection. This feature provides increased stability to the compound when administered orally as a therapeutic agent. This feature further provides for increased specificity and potency as compared to non-cyclized analogs.

In one embodiment, the present invention includes a peptide dimer compound comprising two linked monomer subunits of Formula (I):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-XaA¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴   (Formula (I))

or a pharmaceutically acceptable salt thereof,

wherein:

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid; Xaa⁴ is any amino acid capable of forming a bond with Xaa¹⁰; Xaa⁵ is selected from the group consisting of: N-Me-Arg, Arg, N-Me-Lys, Phe(4-guanidinoguanidino), Phe(4-carbomyl), Cit, Phe(4-NH₂), N-Me-homoArg, homoArg, Tyr, Dap, Dab, Arg-Me-sym, Arg-Me-asym, Cav, and His;

Xaa⁶ is Ser, Gly, Thr or Ile; Xaa⁷ is Asp, Asp(OMe) or N-Me-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu, Gln, Ser, Asp, Pro, Gly, His, Ala, Phe, Lys, Arg, Asn, Glu, Tyr, Trp, Met, Nle, and N-methyl amino acids, including N-Me-Thr; Xaa⁹ is selected from the group consisting of: Gln, Ser, Asp, Pro, Gly, Ala, Phe, Glu, Ile, Val, N-butyl Ala, N-pental Ala, N-hexyl Ala, cyclobutyl Ala, cyclopentylAla, Leu, Nle, Cba, homoLeu, Cpa, Aoc, and N-Me-Leu; Xaa¹⁰ is any amino acid capable of forming a bond with Xaa⁴; Xaa¹¹ is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, and Tic; Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, Aic, Gln, Cit, Glu(OMe), Asn, D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-Tyr, D-Lys, D-Ile, D-His, N-Me-Glu, N-Me-Asp, alpha-homoGlu, Biphenyl-Gly, Biphenyl-Ala, Homo-Phe, D-1-Nal, D-2-Nal, Thr, and Val, and corresponding D-amino acids and isosteres; Xaa¹³ is absent or Pro or any amino acid; and Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, HomoGlu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp; wherein Xaa⁴ and Xaa¹⁰ are both Pen or Cys; wherein: Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomylamino), and N-Me-homoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gin, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; orXaa¹³ is Pro; and wherein one or both monomer subunits of the peptide dimer compound comprises a bond between Xaa⁴ and Xaa¹⁰.

In one embodiment, Xaa⁴ is Cys or Pen, Xaa¹⁰ is Pen or Cys, and Xaa⁴ and Xaa¹⁰ are linked by a disulfide bond.

In particular embodiments of compounds comprising Formula (I), the compound further comprises a linker moiety linking the two monomer subunits, wherein the linker moiety is optionally selected from the group consisting of DIG, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Isovaleric acid, Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, cyclopropylacetic acid, 4-fluoorobenzoic acid, 4-fluorophenylacetic acid, 3-phenylpropionic acid, succinic acid, biotin, glutaric acid, Azelaic acid, Pimelic acid, Dodecanedioic acid, aliphatic amino acids, aromatic amino acids, heteroaromatics, polyethylene glycols having a molecular weight from approximately 400 Da to approximately 40,000 Da, bifunctional linkers, N-Hydroxy succinamine (NHS)-activated diesters, and bis-maleimides.

In particular embodiments compounds comprising Formula I, the N-terminus of each monomer subunit is linked by the linker moiety to provide an N-terminus dimer compound.

In particular embodiments, the C-terminus of each monomer subunit is joined by the linker moiety to provide a C-terminus dimer compound.

In particular embodiments, Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser, Xaa⁷ is Asp, Xaa⁸ is Thr, and/or Xaa⁹ is Leu; aXaa¹¹ is Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), or Phe(4-tBu). In one embodiment, Xaa⁵ is N-Methyl-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹¹ is selected from the group consisting of Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3 diPhenyl Ala, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCL), Phe(3,4-diCL), Phe(4-carbomyl), Phe(3-Carbomyl), Tyr(Me), and HomoPhe; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is selected from the group consisting of: D-Lys, N-Me-Lys, and D-N-Me-Lys.

In particular embodiments, Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Orn, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, HomoGlu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In particular embodiments, Xaa¹⁴ also includes D-Cys and D-Pen. In certain embodiments, Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, Cys, homoCys, Pen and D-Om.

In certain embodiments of Formula (I), Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomylamino), and N-Me-homoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro.

In certain embodiments of Formula (I), one or both monomer subunits of the peptide dimer compound comprises a disulfide bond, a lactam bond, an olefin bond, a 1,2,3-triazole ring, a selenoether bond, or a diselenide bond between Xaa⁴ and Xaa¹⁰.

In certain embodiments, Formula (I) represents a monomer subunit of a dimer molecule, wherein the monomer subunits are linked to form a dimer molecule in accordance with the present invention.

In certain embodiments, Xaa⁴ is Cys or Pen. In certain embodiments, Xaa¹⁰ is Cys or Pen. In certain embodiments, both Xaa⁴ and Xaa¹⁰ are Cys or Pen. In certain embodiments, Both Xaa⁴ and Xaa¹⁰ are Pen. In certain embodiments, the amino acid residue directly C-terminal to Xaa¹⁰ is an aromatic amino acid.

In certain embodiments wherein the compound is a peptide dimer, Xaa¹⁴ is any amino acid with amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, or D-Om. In certain embodiments, Xaa¹⁴ is Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, or D-Om. In certain embodiments, Xaa¹⁴ is Cys, HomoCys, or Pen.

In certain embodiments, one or both monomer subunits of the peptide dimer comprise an intramolecular bind between Xaa⁴ and Xaa¹⁰. In particular embodiments, the intramolecular bond is a disulfide bond or a lactam bond.

In certain embodiments, a free amine in the C-terminal amino acid of the peptide monomer is capped, e.g., with an acetyl group

For some embodiments, any of Xaa¹-Xaa⁵, Xaa⁷-Xaa⁹, and Xaa¹¹-Xaa¹² are N(alpha)Methylated. Xaa⁵ may further be Arg-Me-sym or Arg-Me-asym, and Xaa¹¹ may be O-Me-Tyr, N-Me-Lys(Ac), or 4-Me-Phe. In some instances, any of Xaa¹-Xaa⁴, and Xaa¹¹-Xaa¹⁴ are acylated. For example, in some instances one or more residues at positions Xaa¹-Xaa⁴, and Xaa¹¹-Xaa¹⁴ are acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, and/or Asp are used as spacers for acylations. In some instances, Glu or Asp are used as spacers for acylations.

In some embodiments, the N-terminal or C-terminal amino acids of both peptide monomer subunits of a peptide dimer, e.g., Xaa¹, Xaa², Xaa³, Xaa¹², Xaa¹³ or Xaa¹⁴, are modified with a suitable linker moiety to form a homo- or hetero-dimer molecule, wherein Formula (I) comprises a dimer formed from two subunits joined by a suitable C- or N-terminal linker.

In certain embodiments of Formula (I), both subunits comprise one of the following sequences:

(SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); (SEQ ID NO: 220) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 221) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys); (SEQ ID NO: 222) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 224) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys); (SEQ ID NO: 225) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 226) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys);  (SEQ ID NO: 227) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 228) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 229) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); or (SEQ ID NO: 230) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys).

In certain embodiments, both subunits comprise the same sequences. In particular embodiments, the subunits are linked via DIG at their C-termini.

In particular embodiments the peptide dimer compound has one of the following structures:

(SEQ ID NO: 213) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 130) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 215) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 137) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 231) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 138) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 218) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 149) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 141) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 232) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 231) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 142) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 213) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 214) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 233) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 234) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 235) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 236) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 237) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 238) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 239) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 240) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 241) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 242) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 237) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 243) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 233) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-OH]₂-DIG; or  (SEQ ID NO: 244) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)-OH]₂-DIG, wherein there is a disulfide bond between the two Pen residues in the monomer subunits.

In particular embodiments, the peptide dimer compound comprises an C-terminal OH.

In particular embodiments, the peptide dimer compound comprises N(alpha)methylation at one or more positions selected from the group consisting of Xaa³, Xaa⁵, Xaa⁷-Xaa⁹, and Xaa¹¹-Xaa¹³; or acylation at one or more position selected from the group consisting of Xaa¹-Xaa³ and Xaa¹¹-Xaa¹⁴. In one embodiment, Xaa¹ and Xaa² are absent, and Xaa³ is Ac. In one embodiment, one or more of Xaa¹¹, Xaa¹² and Xaa¹³ is absent.

In a related embodiment, the present invention includes a peptide monomer compound of Formula (IV):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴   (Formula (IV))

or a pharmaceutically acceptable salt thereof,

wherein:

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid; Xaa⁴ is any amino acid capable of binding to Xaa¹⁰; Xaa⁵ is selected from the group consisting of: N-Me-Arg, Arg, N-Me-Lys, Phe(4-guanidino), Phe(4-carbomylamino), Cit, Phe(4-NH₂), N-Me-homoArg, homoArg, Tyr, Dap, Dab, Arg-Me-sym, Arg-Me-asym, Cav, and His;

Xaa⁶ is Ser, Gly, Thr, or Ile; Xaa⁷ is Asp, Asp(OMe), or N-Me-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu, Gln, Ser, Asp, Pro, Gly, His, Ala, Phe, Lys, Arg, Asn, Glu, Tyr, Trp, Met, Nle, and N-methyl amino acids, including N-Me-Thr; Xaa⁹ is selected from the group consisting of: Gln, Ser, Asp, Pro, Gly, Ala, Phe, Glu, Ile, Val, N-butyl Ala, N-pental Ala, N-hexyl Ala, cyclobutyl Ala, cyclopentylAla, Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu; Xaa¹⁰ is any amino acid capable of binding to Xaa⁴; Xaa¹¹ is absent or selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenyl Ala, Tic, b-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-Carbomyl), Phe(2-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, Dihydro Trp, Ile, Leu, Arg, Thr, aromatic amino acids, substituted aromatic amino acids, and Tic; Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, Aic, Gln, Cit, Glu(OMe), Asn, D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-Tyr, D-Lys, D-Ile, D-His, N-Me-Glu, N-Me-Asp, alpha-homoGlu, Biphenyl-Gly, Biphenyl-Ala, Homo-Phe, D-1-Nal, D-2-Nal, Thr, and Val, and corresponding D-amino acids and isosteres; Xaa¹³ is absent or Pro or any amino acid; and Xaa¹⁴ is any amino acid, wherein Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-HomoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or

Xaa¹³ is Pro;

wherein Xaa⁴ and Xaa¹⁰ are linked by a bond; and

wherein

Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-HomoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or

Xaa¹³ is Pro.

In particular embodiments, Xaa⁴ is Cys or Pen, Xaa¹⁰ is Cys or Pen, and Xaa⁴ and Xaa¹⁰ are linked by a disulfide bond.

In particular embodiments, Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, and corresponding D-amino acids and suitable isosteres.

In particular embodiments, Xaa¹³ is absent or Pro.

In particular embodiments, Xaa⁵ is N-Me-Arg.

In particular embodiments, Xaa¹ and Xaa² are absent, and Xaa³ is Ac, and/or wherein one or more of Xaa¹¹, Xaa¹² and Xaa¹³ is absent.

In particular embodiments of Formula (IV), Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-HomoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro.

In particular embodiments, the peptide monomer compound comprises a disulfide bond, a lactam bond, an olefin bond, a 1,2,3-triazole ring, a selenoether bond, or a diselenide bond between Xaa⁴ and Xaa¹⁰.

In certain embodiments, a monomer peptide comprises a disulfide bond, a lactam bond, an olefin bond, a 1,2,3-triazole ring, a selenoether bond, or a diselenide bond between Xaa⁴ and Xaa¹⁰.

In certain embodiments, Xaa⁴ is Cys or Pen. In certain embodiments, Xaa¹⁰ is Cys or Pen. In certain embodiments, both Xaa⁴ and Xaa¹⁰ are Cys or Pen. In certain embodiments, both Xaa⁴ and Xaa¹⁰ are Pen.

In certain embodiments, the amino acid residue directly C-terminal to Xaa¹⁰ is an aromatic amino acid.

In certain embodiments, Xaa¹⁴ or the C-terminal amino acid does not comprise a free amine.

In certain embodiments, Xaa¹⁴ is absent or any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, or D-Om. In certain embodiments, Xaa¹⁴ is Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, or D-Orm.

In certain embodiments wherein the compound is peptide monomer, Xaa¹⁴ or the C-terminus comprises an NH₂ or an OH.

In certain embodiments, a free amine in the C-terminal amino acid of the peptide monomer is capped, e.g., with an acetyl group.

In certain embodiments, the peptide monomer comprises an intramolecular bind between Xaa⁴ and Xaa¹⁰. In particular embodiments, the intramolecular bond is a disulfide bond or a lactam bond.

For some embodiments, any of Xaa¹-Xaa⁵, Xaa⁷-Xaa⁹, and Xaa¹¹-Xaa¹² are N(alpha)Methylated. Xaa⁵ may further be Arg-Me-sym or Arg-Me-asym, and Xaa¹¹ may be O-Me-Tyr, N-Me-Lys(Ac), or 4-Me-Phe. In some instances, any of Xaa¹-Xaa⁴, and Xaa¹¹-Xaa¹⁴ are acylated. For example, in some instances one or more residues at positions Xaa¹-Xaa⁴, and Xaa¹¹-Xaa¹⁴ are acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations.

The invention also includes a peptide monomer compound of Formula (V):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰   (Formula (V))

or a pharmaceutically acceptable salt thereof,

wherein the peptide compound comprises a disulfide bond Xaa¹ and Xaa;

wherein Xaa¹-Xaa¹⁰ of Formula (V) corresponds to Xaa⁴-Xaa³ of Formula (IV), and

wherein

Xaa¹ is Pen or Cys;

Xaa² is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-HomoArg

Xaa³ is Ser, Gly, Thr, or Ile; Xaa⁴ is Asp, D-Asp, Asp(OMe), or N-Me-Asp;

Xaa⁵ is selected from the group consisting of Leu, HomoLeu, Nle and Val; Xaa⁶ is selected from the group consisting of: Cba, HomoLeu, and Cpa;

Xaa⁷ is Pen or Cys;

Xaa⁸ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa⁹ is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; and

Xaa¹⁰ is Pro.

In certain embodiments, the peptide monomer compound comprises one of the following sequences or structures:

(SEQ ID NO: 245) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH))-(Glu)-(D-Lys); (SEQ ID NO: 220) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH))-(β-homo-Glu)-(D-Lys); (SEQ ID NO: 246) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-tBu))-Glu-(D-Lys); (SEQ ID NO: 247) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-tBu))-(β-homo-Glu)-(D-Lys); (SEQ ID NO: 248) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-tBu))-Glu-(N-Me-Lys); (SEQ ID NO: 249) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Bip-Glu-(D-Lys); (SEQ ID NO: 250) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Bip-(β-homo-Glu)-(D-Lys); (SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); (SEQ ID NO: 220) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 221) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys); (SEQ ID NO: 222) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 224) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys); (SEQ ID NO: 225) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 226) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 227) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 228) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 229) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); (SEQ ID NO: 230) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys); (SEQ ID NO: 251) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 252) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH)-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 253) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)-OH; (SEQ ID NO: 254) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 255) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 256) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys)-OH; (SEQ ID NO: 257) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 258) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)-OH; (SEQ ID NO: 259) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)-OH; (SEQ ID NO: 260) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)-OH; (SEQ ID NO: 255) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 261) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)-OH; (SEQ ID NO: 251) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 262) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)-OH; (SEQ ID NO: 263) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 264) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 265) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)-NH₂; (SEQ ID NO: 266) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 267) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 268) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(M-Me-Lys)-NH₂; (SEQ ID NO: 153) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 269) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)-NH₂; (SEQ ID NO: 270) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)-NH₂; (SEQ ID NO: 271) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)-NH₂; (SEQ ID NO: 267) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 272) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)-NH₂; (SEQ ID NO: 263) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 273) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)-NH₂; or (SEQ ID NO: 274) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH))-(Glu); (SEQ ID NO: 275) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH)-(β-homo-Glu); (SEQ ID NO: 276) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-tBu))-Glu; (SEQ ID NO: 277) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-tBu))-(β-homo-Glu); (SEQ ID NO: 276) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-tBu))-Glu; (SEQ ID NO: 278) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Bip-Glu; (SEQ ID NO: 279) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Bip-(β-homo-Glu); (SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu); (SEQ ID NO: 275) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH))-(β-homoGlu); (SEQ ID NO: 281) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu; (SEQ ID NO: 282) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu); (SEQ ID NO: 284) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu; (SEQ ID NO: 285) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu); (SEQ ID NO: 285) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu); (SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu); (SEQ ID NO: 282) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu); (SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu); (SEQ ID NO: 281) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu; (SEQ ID NO: 146) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-OH; (SEQ ID NO: 286) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-OH; (SEQ ID NO: 128) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-OH; (SEQ ID NO: 287) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-OH; (SEQ ID NO: 288) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-OH; (SEQ ID NO: 289) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-OH; (SEQ ID NO: 152) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-OH; (SEQ ID NO: 152) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-OH; (SEQ ID NO: 146) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-OH; (SEQ ID NO: 287) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-OH; (SEQ ID NO: 288) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-OH; (SEQ ID NO: 288) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-OH; (SEQ ID NO: 146) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-OH; (SEQ ID NO: 128) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-OH; (SEQ ID NO: 290) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-NH₂; (SEQ ID NO: 291) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-NH₂; (SEQ ID NO: 292) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-NH₂; (SEQ ID NO: 155) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-NH₂; (SEQ ID NO: 293) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-NH₂; (SEQ ID NO: 294) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-NH₂; (SEQ ID NO: 165) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-NH₂; (SEQ ID NO: 165) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-NH₂; (SEQ ID NO: 290) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-NH₂; (SEQ ID NO: 155) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-NH₂; (SEQ ID NO: 293) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-NH₂; (SEQ ID NO: 293) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-NH₂; (SEQ ID NO: 290) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-NH₂; or (SEQ ID NO: 292) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-NH₂, wherein in certain embodiments, there is a disulfide bond between the two Pen residues of the peptide or peptide monomer compound.

In certain embodiments, any of the compounds are detectably labeled.

The present invention further includes pharmaceutical composition comprising any of the compounds of the invention. In one embodiment, the pharmaceutical composition comprises an enteric coating, wherein the enteric coating protects and releases the pharmaceutical composition within a subject's lower gastrointestinal system

The invention further includes a method for treating a subject afflicted with a condition that is associated with a biological function of an α4β7 integrin, the method comprising administering to the human an effective amount of a compound or compoids of the present invention.

In certain embodiments, the condition is selected from the group consisting of Inflammatory Bowel Disease (IBD), ulcerative colitis, Crohn's disease, Celiac disease (nontropical Sprue), enteropathy associated with seronegative arthropathies, microscopic colitis, collagenous colitis, eosinophilic gastroenteritis, radiotherapy, chemotherapy, pouchitis resulting after proctocolectomy and ileoanal anastomosis, gastrointestinal cancer, pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, pericholangitis, chronic bronchitis, chronic sinusitis, asthma, primary sclerosing cholangitis, human immunodeficiency virus (HIV) infection in the GI tract, eosinophilic asthma, eosinophilic esophagitis, gastritis, colitis, microscopic colitis, graft versus host disease, colitis associated with radio- or chemo-therapy, colitis associated with disorders of innate immunity as in leukocyte adhesion deficiency-1, chronic granulomatous disease, glycogen storage disease type 1b, Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, and Wiskott-Aldrich Syndrome, or pouchitis resulting after proctocolectomy and ileoanal anastomosis and various forms of gastrointestinal cancer, osteoporosis, arthritis, multiple sclerosis, chronic pain, weight gain, and depression. In another embodiment, the condition is pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, pericholangitis, chronic bronchitis, chronic sinusitis, asthma or graft versus host disease. In particular embodiments, the condition is an inflammatory bowel disease, such as ulcerative colitis or Crohn's disease.

In particular embodiments, the peptide dimer compound or peptide monomer compound of the invention inhibits binding of α4β7 to MAdCAM, and/or selectively inhibits binding of α4β7 to MAdCAM.

In certain embodiments, the subject is a human.

In certain embodiments, the peptide dimer compound or peptide monomer compound is administered by a form of administration selected from the group consisting of oral, intravenous, peritoneal, intradermal, subcutaneous, intramuscular, intrathecal, inhalation, vaporization, nebulization, sublingual, buccal, parenteral, rectal, vaginal, and topical.

In particular embodiments, the peptide dimer compound or peptide monomer compound is administered as an initial does followed by one or more subsequent doses and the minimum interval between any two doses is a period of less than 1 day, and wherein each of the doses comprises an effective amount of the peptide dimer compound.

In particular embodiments, the effective amount of peptide dimer compound or peptide monomer compound is sufficient to achieve at least one of the following selected from the group consisting of: a) about 50% or greater saturation of MAdCAM binding sites on α4β7 integrin molecules; b) about 50% or greater inhibition of α4β7 integrin expression on the cell surface; and c) about 50% or greater saturation of MAdCAM binding sites on α4β7 molecules and about 50% or greater inhibition of α4β7 integrin expression on the cell surface, wherein i) the saturation is maintained for a period consistent with a dosing frequency of no more than twice daily; ii) the inhibition is maintained for a period consistent with a dosing frequency of no more than twice daily; or iii) the saturation and the inhibition are each maintained for a period consistent with a dosing frequency of no more than twice daily.

In particular embodiments, the compound or pharmaceutical composition is administered orally, parenterally, or topically. In particular embodiments, it is administered at an interval selected from the group consisting of around the clock, hourly, every four hours, once daily, twice daily, three times daily, four times daily, every other day, weekly, bi-weekly, and monthly.

BRIEF DESCRIPTION OF THE DRAWINGS

In order that the manner in which the above-recited and other features and advantages of the invention are obtained will be readily understood, a more particular description of the invention briefly described above will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings. Understanding that these drawings depict only typical embodiments of the invention and are not therefore to be considered to be limiting of its scope, the invention will be described and explained with additional specificity and detail through the use of the accompanying drawings.

FIG. 1 is a schematic showing C and N-terminal dimerizations.

FIG. 2 is a schematic showing a pair of integrin antagonist monomer subunits (SEQ ID NOs: 348 and 349, respectively, in order of appearance), wherein the subunits are aligned and linked at their respective C-termini by a DIG linker in accordance with a representative embodiment of the present invention.

FIGS. 3A and 3B provide schematics, each showing a pair of integrin antagonist monomer subunits wherein the subunits are aligned and linked at their respective C-termini (3A) or N-termini (3B) by a linker. In certain embodiments, the linker connects two sulfur-containing amino-acids to form a peptide dimer compound. The two sulfur containing amino acids may be connected by a linker comprising a di-halide, an aliphatic chain, or a PEG. For example, the linker can connect two monomeric subunits by connecting sulfur containing C-terminal amino acids at the C-terminus of each monomer subunit, or it can connect two monomer subunits by connecting sulfur containing N-terminal amino acids at the N-terminus of each monomer subunit. In certain embodiments, the linker connects two amine-containing amino acids to form a peptide dimer compound. The two amine-containing amino acids may be connected by a linker, e.g., comprising a di-halide, an aliphatic chain, or a PEG. For example, the linker can connect two monomeric subunits by connecting amine-containing C-terminal amino acids at the C-terminus of each monomer subunit, or it can connect two monomer subunits by connecting amine-containing N-terminal amino acids at the N-terminus of each monomer subunit.

FIG. 4 shows the structure of Peptide X.

FIG. 5 provides a summary of stability data generated for Peptide X, demonstrating that Peptide X is stable to a variety of GI fluids, metabolic enzymes and intestinal bacteria.

FIG. 6 shows the results of pre-clinical animal studies of Peptide X, showing dose proportional PK-PD-efficacy correlations in colitis mice.

FIGS. 7A and 7B provide graphs showing the binding specificities of Peptide X and vedolizumab to various cells in human whole blood as measured by FACS. For each cell type, vedolizumab results are shown in the top graph, and Peptide X results are shown in the bottom graph.

FIG. 8 is a graph showing mean endoscopy score of DSS mice treated with vehicle or Peptide X.

FIG. 9 provides endoscopy images from vehicle control or Peptide X treated DSS mice. A normal control from a different study is also shown. The white circle indicates colonic friability.

FIGS. 10A and 10B are graphs showing the total α4β7+ memory cells following treatment with vehicle or Peptide X in blood (A) and spleen (B). α4β7+ memory T cells are defined as CD4+, CD45RB^(low), CD44^(high), α4β7⁺. Data are presented as mean±SEM. n=10 mice per group.

FIGS. 11A and 11B are graphs showing the percent α4β7 memory cells relative to total cells in the MLN (A) and Peyer's Patches (B). α4β7+ memory T cells are defined as CD4+, CD45RB^(low), CD44^(high), α4β7⁺. Data are presented as mean±SEM. N=1-mice per group.

FIG. 12 is a graph showing the exposure of Peptide X in the plasma, proximal colon and distal colon following oral administration.

FIGS. 13A-13D provide graphs showing the amount of α4β7+ memory T cells in Peyer's patches (A), blood (B), MLN (C) and spleen (D) in the mouse DSS colitis model. Peyer's patches, MLN, spleen and blood were collected and levels of α4β7+ memory T cells analyzed by FACS. Data is presented as means and SD. N=10 mice per group. Statistical significance was assessed by one-way ANOVA: *:p≤0.05; **:p≤0.01. Percentage values and statistical significance are relative to vehicle control.

FIG. 14 is a graph showing percent receptor occupancy of CD4 memory α4β7+ T cells by Peptide X after 7 days dosing in cyno monkeys. For each animal, the percent receptor occupancy at Day 6 was normalized to the pre-dose control at Day 0.

FIG. 15 is a graph showing the percent receptor occupancy versus Peptide X plasma concentration for each animal.

FIG. 16 is graph showing expression of α4β7 on CD4 memory T cells in cyno blood. Shown is the mean fluorescence intensity (MFI) at Day 6 normalized to the pre-dose control at Day 0 for each animal.

FIGS. 17A and 17B are graphs showing the percent increase in circulating α4β7 memory T cells normalized to total CD4 cells in cyno blood.

FIGS. 18A-18D provide graphs showing that Peptide XX reduces colon macroscopic histopathology scores comparable to antibodies in a murine 15 day chronic DSS model. *Gross colon score evaluated by a pathologist (0=normal, 1=erythema, 2=erythema, slight edema and small erosions, 3=two or more bleeding ulcers, inflammation, and moderate adhesions, 4=severe ulceration, stenosis with dilation and severe adhesions).

FIGS. 19A and 19B show that Peptide XX reduced infiltration of f37+ cells into the lumina propria of the distal colon in the 15 day chronic DSS colitis model. Data is represented as means and SD. N=10 mice per group. Statistical significance relative to vehicle control assessed by one-way ANOVA: *:p≤0.05; **:p≤0.005; ***:p≤0.0001; ns: not significant.

FIG. 20 is a schematic showing an integrin antagonist peptide (SEQ ID NO: 348), wherein Xaa⁴ and Xaa¹⁰ are connected by a disulfide bond.

FIG. 21 shows immunohistochemistry of PFA fixed small intestine tissue samples obtained from an animal treated with 10 mg/kg or 90 mg/kg of Peptide X conjugated to Alex 488, stained with an anti-Alex 488 antibody.

FIG. 22 provides a graph showing that treatment with Peptide X in a chronic model of DSS resulted in reduced infiltration of α4β7+B cells into the lamina propia.

DETAILED DESCRIPTION

The present invention relates generally to peptides that have been shown to have integrin antagonist activity, including both peptide monomer compounds and peptide dimer compounds. As demonstrated herein, peptides of the present invention are selective antagonists of α4β7 integrin with minimal systemic exposure when administered orally, and are effective in blocking T cell homing and preventing mucosal damage in murine models of IBD. In murine colitis models, peptide compounds of the present invention blocked T cell trafficking and reduce histopathology.

In particular embodiments, the present invention relates to various peptide monomer compounds or peptide dimer compounds comprising hetero- or homo-monomer subunits, which form cyclized structures through a disulfide bond, lactam bond, olefin bond, triazole bond, selenoether bond or diselenide bond. In certain embodiments, a peptide monomer compounds or one or both monomer subunits of a peptide dimer compound comprises an intramolecular bond to form a cyclized peptide monomer compound or cyclized monomer subunit. The cyclized structure of peptide monomer compounds and monomer subunits of peptide dimer compounds has been shown to increase potency and selectivity, and also increase stability for oral delivery. A non-limiting, representative illustration of the cyclized structure of a peptide monomer subunit and peptide dimer compound is shown in FIG. 2.

Definitions

As used herein, the singular forms “a,” “and” and “the” include plural references unless the context clearly dictates otherwise.

As used in the present specification the following terms have the meanings indicated:

The term “peptide,” as used herein, refers broadly to a sequence of two or more amino acids joined together by peptide bonds. It should be understood that this term does not connote a specific length of a polymer of amino acids, nor is it intended to imply or distinguish whether the polypeptide is produced using recombinant techniques, chemical or enzymatic synthesis, or is naturally occurring.

The term “DRP,” as used herein, refers to disulfide rich peptides.

The term “dimer,” as used herein, refers broadly to a peptide comprising two or more subunits, wherein the subunits are peptides, e.g., DRPs, linked at their C- or N-termini. Dimers also include peptides comprising two subunits that are linked via one or more internal amino acid residues or derivatives thereof. Each of the subunits may be linked to the other via its N-terminus, C-terminus, or through an internal amino acid or derivate thereof, which may be different for each of the two subunits. Dimers of the present invention may include homodimers and heterodimers and function as integrin antagonists. Peptide dimer compounds may be described herein using the following nomenclature: [X_(n)]₂, which indicates that the peptide dimer comprises two monomer subunits defined within the brackets (e.g., X_(n), where X represents an amino acid and n indicates the number of amino acids in the peptide). A linker moiety linking the two peptide subunits may be shown as follows: [X_(n)]₂-L or L-[X_(n)]₂, where L is the linker. Other chemical moieties, such as detectable labels may be shown in a similar manner as for the linker.

The term “L-amino acid,” as used herein, refers to the “L” isomeric form of an amino acid, and conversely the term “D-amino acid” refers to the “D” isomeric form of an amino acid. The amino acid residues described herein are preferred to be in the “L” isomeric form, however, residues in the “D” isomeric form can be substituted for any L-amino acid residue, as long as the desired functional is retained by the peptide.

The term “NH₂,” as used herein, refers to the free amino group present at the amino terminus of a polypeptide. The term “OH,” as used herein, refers to the free carboxy group present at the carboxy terminus of a peptide. Further, the term “Ac,” as used herein, refers to Acetyl protection through acylation of the C- or N-terminus of a polypeptide, or any amino acid in the peptide. The term “NH₂” may also be used herein to refer to a C-terminal amide group, e.g., in the context of a CONH₂.

The term “carboxy,” as used herein, refers to —CO₂H.

The term “isostere” or “isostere replacement,” as used herein, refers to any amino acid or other analog moiety having physiochemical and/or structural properties similar to a specified amino acid. In particular embodiments, an “isostere” or “suitable isostere” of an amino acid is another amino acid of the same class, wherein amino acids belong to the following classes based on the propensity of the side chain to be in contact with polar solvent like water: hydrophobic (low propensity to be in contact with water), polar or charged (energetically favorable contact with water). Illustrative charged amino acid residues include lysine (+), arginine (+), aspartate (−) and glutamate (−). Illustrative polar amino acids include serine, threonine, asparagine, glutamine, histidine and tyrosine. Illustrative hydrophobic amino acids include alanine, valine, leucine, isoleucine, proline, phenylalanine, tryptophane, cysteine and methionine. The amino acid glycine does not have a side chain and is hard to assign to one of the above classes. However, glycine is often found at the surface of proteins, often within loops, providing high flexibility to these regions, and an isostere may have a similar feature. Proline has the opposite effect, providing rigidity to the protein structure by imposing certain torsion angles on the segment of the polypeptide chain. In certain embodiments, an isostere is a derivative of an amino acid, e.g., a derivative having one or more modified side chains as compared to the reference amino acid.

The term “cyclized,” as used herein, refers to a reaction in which one part of a polypeptide molecule becomes linked to another part of the polypeptide molecule to form a closed ring, such as by forming a disulfide bridge or other similar bond, e.g. a lactam bond. In particular embodiments, peptide monomer compounds or monomer subunits of peptide dimer compounds described herein are cyclized via an intramolecular bond between two amino acid residues present in the peptide monomer or monomer subunit.

The term “subunit,” as used herein, refers to one of a pair of polypeptides monomers that are joined at the C- or N-terminus to form a dimer peptide composition.

The term “linker,” as used herein, refers broadly to a chemical structure that is capable of linking together a plurality of peptide monomer subunits to form a dimer.

The term “receptor,” as used herein, refers to chemical groups of molecules on the cell surface or in the cell interior that have an affinity for a specific chemical group or molecule. Binding between dimer peptides and targeted integrins can provide useful diagnostic tools.

The term “integrin-related diseases,” as used herein, refer to indications that manifest as a result of integrin binding, and which may be treated through the administration of an integrin antagonist.

As used herein, the terms “disease,” “disorder,” and “condition” may be used interchangeably.

As used herein, “inhibition,” “treatment,” “treating,” and “ameliorating” are used interchangeably and refer to, e.g., stasis of symptoms, prolongation of survival, partial or full amelioration of symptoms, and partial or full eradication of a condition, disease or disorder in a subject, e.g., a mammal.

As used herein, ‘prevent” or “prevention” includes (i) preventing or inhibiting the disease, injury, or condition from occurring in a subject, e.g., a mammal, in particular, when such subject is predisposed to the condition but has not yet been diagnosed as having it; or (ii) reducing the likelihood that the disease, injury, or condition will occur in the subject.

The term “pharmaceutically acceptable salt,” as used herein, represents salts or zwitterionic forms of the compounds of the present invention which are water or oil-soluble or dispersible, which are suitable for treatment of diseases without undue toxicity, irritation, and allergic response; which are commensurate with a reasonable benefit/risk ratio, and which are effective for their intended use. The salts can be prepared during the final isolation and purification of the compounds or separately by treatment of an amino group with a suitable acid. Representative acid addition salts include acetate, adipate, alginate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsulfonate, digluconate, glycerophosphate, hemisulfate, heptanoate, hexanoate, formate, fumarate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethansulfonate (isethionate), lactate, maleate, mesitylenesulfonate, methanesulfonate, naphthylenesulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, pamoate, pectinate, persulfate, 3-phenylproprionate, picrate, pivalate, propionate, succinate, tartrate, trichloroacetate, trifluoroacetate, phosphate, glutamate, bicarbonate, para-toluenesulfonate, and undecanoate. Also, amino groups in the compounds of the present invention can be quatemized with methyl, ethyl, propyl, and butyl chlorides, bromides, and iodides; dimethyl, diethyl, dibutyl, and diamyl sulfates; decyl, lauryl, myristyl, and steryl chlorides, bromides, and iodides; and benzyl and phenethyl bromides. Examples of acids which can be employed to form therapeutically acceptable addition salts include inorganic acids such as hydrochloric, hydrobromic, sulfuric, and phosphoric, and organic acids such as oxalic, maleic, succinic, and citric. In certain embodiments, any of the peptide momoner compounds or peptide dimer compounds described herein are salt forms, e.g., acetate salts.

The term “N(alpha)Methylation”, as used herein, describes the methylation of the alpha amine of an amino acid, also generally termed as an N-methylation.

The term “sym methylation” or “Arg-Me-sym”, as used herein, describes the symmetrical methylation of the two nitrogens of the guanidine group of arginine. Further, the term “asym methylation” or “Arg-Me-asym” describes the methylation of a single nitrogen of the guanidine group of arginine.

The term “acylating organic compounds”, as used herein refers to various compounds with carboxylic acid functionality e.g. which may be used to acylate the N-terminus of an amino acid subunit prior to forming a C-terminal dimer. Non-limiting examples of acylating organic compounds include cyclopropylacetic acid, 4-Fluorobenzoic acid, 4-fluorophenylacetic acid, 3-Phenylpropionic acid, Succinic acid, Glutaric acid, Cyclopentane carboxylic acid, 3,3,3-trifluoropropeonic acid, 3-Fluoromethylbutyric acid, Tetrahedro-2H-Pyran-4-carboxylic acid.

All peptide sequences are written according to the generally accepted convention whereby the α-N-terminal amino acid residue is on the left and the α-C-terminal is on the right. As used herein, the term “α-N-terminal” refers to the free α-amino group of an amino acid in a peptide, and the term “α-C-terminal” refers to the free α-carboxylic acid terminus of an amino acid in a peptide. Peptide sequences may be shown in tables, which may further disclose additional moieties, such as N-terminal or C-terminal chemical modifications, linkers, conjugates, and/or labels, which are present in certain embodiments of the compounds of the invention.

It is noted that the term “comprising” is intended to be open and permits but does not require the inclusion of additional elements or steps. When the term “comprising” is used herein, the term “consisting of” is thus also encompassed and disclosed.

The term “amino acid” or “any amino acid” as used here refers to any and all amino acids, including naturally occurring amino acids (e.g., α-amino acids), unnatural amino acids, modified amino acids, and non-natural amino acids. It includes both D- and L-amino acids. Natural amino acids include those found in nature, such as, e.g., the 23 amino acids that combine into peptide chains to form the building-blocks of a vast array of proteins. These are primarily L stereoisomers, although a few D-amino acids occur in bacterial envelopes and some antibiotics. The “non-standard,” natural amino acids are pyrrolysine (found in methanogenic organisms and other eukaryotes), selenocysteine (present in many noneukaryotes as well as most eukaryotes), and N-formylmethionine (encoded by the start codon AUG in bacteria, mitochondria and chloroplasts). “Unnatural” or “non-natural” amino acids are non-proteinogenic amino acids (i.e., those not naturally encoded or found in the genetic code) that either occur naturally or are chemically synthesized. Over 140 natural amino acids are known and thousands of more combinations are possible. Examples of “unnatural” amino acids include β-amino acids (β³ and β²), homo-amino acids, proline and pyruvic acid derivatives, 3-substituted alanine derivatives, glycine derivatives, ring-substituted phenylalanine and tyrosine derivatives, linear core amino acids, diamino acids, D-amino acids, alpha-methyl amino acids and N-methyl amino acids. Unnatural or non-natural amino acids also include modified amino acids. “Modified” amino acids include amino acids (e.g., natural amino acids) that have been chemically modified to include a group, groups, or chemical moiety not naturally present on the amino acid.

For the most part, the names of naturally occurring and non-naturally occurring aminoacyl residues used herein follow the naming conventions suggested by the IUPAC Commission on the Nomenclature of Organic Chemistry and the IUPAC-IUB Commission on Biochemical Nomenclature as set out in “Nomenclature of α-Amino Acids (Recommendations, 1974)” Biochemistry, 14(2), (1975). To the extent that the names and abbreviations of amino acids and aminoacyl residues employed in this specification and appended claims differ from those suggestions, they will be made clear to the reader. Some abbreviations useful in describing the invention are defined below in the following Table 1.

TABLE 1 Definitions and Abbreviations Abbreviation Definition DIG DiGlycolic acid (Linker) Dap Diaminopropionic acid Dab Diaminobutyric acid Pen Penicillamine Sar Sarcosine Cit Citroline Cav Cavanine Phe(4-Guanidino) or 4-Guanidine-Phenylalanine 4-Guan N-Me-Arg; N-Methyl-Arginine N(alpha)Methylation Ac- Acetyl 2-Nal 2-Napthylalanine 1-Nal 1-Napthylalanine Bip Biphenylalanine O-Me-Tyr Tyrosine (O-Methyl) N-Me-Lys N-Methyl-Lysine N-Me-Lys (Ac) N-e-Acetyl-D-lysine 3,3-DiphenylAla 3,3 DiPhenylAlanine 3,3-DiphenylGly 3,3-DiphenylGlycine NH₂ Free Amine CONH₂ Amide COOH Acid Phe(4-F) 4-Fluoro-Phenylanine PEG13 Bifunctional PEG linker with 13 PolyEthylene Glycol units PEG25 Bifunctional PEG linker with 25 PolyEthylene Glycol units PEG1K Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 1000Da PEG2K Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 2000Da PEG3.4K Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 3400Da PEG5K Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 5000Da IDA β-Ala-Iminodiacetic acid (Linker) IDA-Palm β-Ala (Palmityl)-Iminodiacetic acid HPhe homo Phenylalanine homoPhe Ahx Aminohexanoic acid Me Methyl Triazine Amino propyl Triazine di-acid Boc-Triazine Boc-Triazine di-acid Trifluorobutyric acid Acylated with 4,4,4-Trifluorobutyric acid 2-Methly-trifluorobutyric acid acylated with 2-Methy-4,4,4-Butyric acid Trifluorpentanoic acid Acylated with 5,5,5-Trifluoropentanoic acid 1,4-Phenylenediacetic acid para-Phenylenediacetic acid (Linker) 1,3-Phenylenediacetic acid meta-Phenylenediacetic acid (Linker) DTT Dithiothreotol Nle Norleucine β-HTrp or β-homoTrypophane β-homoTrp β-HPhe or β-homophenylalanine β-homoPhe Phe(4-CF3) 4-Trifluoromethyl Phenylalanine β-Asp β-Aspartic acid  

β-HGlu beta-homoGlu β-homoglutamic acid  

2-2-Indane 2-Aminoindane-2-carboxylic acid 1-1-Indane 1-Aminoindane-1-carboxylic acid Cpa CyclopentylAlanine Orn Ornithine Aoc 2-Amino octonoic acid Cba Cyclobutyl alanine HCha homocyclohexyl Alanine Cyclobutyl Cyclobutylalanine β-HPhe or P-homophenylalanine β-homoPhe HAsp or HomoAspartic acid homoAsp HLys or homoLysine homoLys HCys or HomoCysteine homoCys HGlu or homoGlutamic acid homoGlu HomoLeu or homoLeucine homoLeu Gla Gama-Carboxy-Glutamic acid Tic (3S-)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid  

Phe(4CF3) Phe(4-trifluoromethyl 3-(4-trifluoromethyl-phenyl)propionic acid Phe(2,4-diCl) (S)-Fmoc-2-amino-3-(2,4-dichlorophenyl)propionic acid Phe(3,4-diCl) (S)-Fmoc-2-amino-3-(3,4-dichlorophenyl)propionic acid Pen(═O) Penicillamine sulfoxide Aic aminoindan-2-carboxylic acid Phe(2-carbomyl) L-2-carbamoylphenylalanine Phe(3-carbomyl) L-3-carbamoylphenylalanine Phe(4-carbomyl) L-4-carbomylphenylalanine Phe(4-COOH) (4-carboxy-tert-butyl)-L-phenylalanine Phe(4-OMe) (S)-4-methoxyphenylalanine Phe(4-tBu) 2-amino-3-(4-tert-butyl-phenyl)propionic acid Phe(4-F) 4-fluoro-L-phenylalanine Glu(OMe) L-glutamic acid g-methyl ester β-azido-Ala-OH β-azido-Alanine Aoc 8-amino-octanoic acid

Aspects of the present invention include peptide dimer compounds comprising two monomer subunits, wherein the peptide dimer compounds are antagonists of α4β7 integrin. Related aspects of the present invention include monomer subunits of peptide antagonists. Monomer subunits present in peptide dimer compounds are linked at either their C- or N-terminus, e.g., as shown in FIG. 1, or via internal amino acid residues, e.g., by a linker moiety. In particular embodiments, both monomer subunits are linked via their respective N-termini, both monomer subunits are linked via their respective C-termini, or both monomer subunits are linked via internal amino acid residues. In further embodiments, one monomer subunit is linked via any of its N-terminus, C-terminus, or an internal amino acid to another monomer subunit via any of its N-terminus, C-terminus or an internal amino acid, and linkages may occur via the same or different amino acid residues on two monomer subunits of a peptide dimer compound. In further related embodiments, monomer subunits of peptide dimer compounds of the present invention are linked via both their N-terminus and their C-terminus. In one embodiments the two N-termini of the monomer subunits are linked; in one embodiment, the two C-termini of the monomer subunits are linked; and in one embodiment, the N-terminus of the first monomer subunit is linked to the C-terminus of the second monomer subunit of a peptide dimer compound, and the C-terminus of the first monomer subunit is linked to the N-terminus of the second monomer subunit of the peptide dimer compound.

The linker moieties of the present invention may include any structure, length, and/or size that is compatible with the teachings herein. In certain embodiments, a linker moiety is selected from the non-limiting group consisting of DIG, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Ac, IDA-Isovaleric acid, ADA Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, Glu, Asp, D-Glu, D-Asp, 1,4-phenylenediacetic acid, Biphenyl diacetic acid, cyclopropylacetic acid, succinic acid, glutaric acid, Dodecanedioic acid, suitable aliphatic diacids, suitable aromatic diacids, heteroaromatics, and polyethylene glycols having a molecular weight from approximately 400 Da to approximately 40,000 Da. When the linker is IDA, ADA or any linker with free amine it can be acylated with acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid, straight chain aliphatic acids with 10 to 20 carbon units, cholic acid and other bile acids. In some instances, small PEG (PEG4-PEG13), Glu, IsoGlu or Asp is used as spacer before acylations.

In certain embodiments, the linker connects two monomer subunits by connecting two sulfur containing C- or N-terminal amino acids. In some embodiments, the two sulfur containing amino acids are connected by a linker comprising a di-halide, an aliphatic chain, or a PEG. In certain embodiments, the linker connects two monomeric subunits by connecting sulfur containing C-terminal amino acids at the C-terminus of each monomer subunit. In certain embodiments, the linker connects two monomeric subunits by connecting sulfur containing N-terminal amino acids at the N-terminus of each monomer subunit. In certain embodiments, the linker connects two monomeric subunits by connecting a sulfur containing C-terminal amino acid of one monomer subunit to a sulfur-containing N-terminal amino acid of the other monomer subunit. In some embodiments, the two sulfur containing amino acids are connected by a linker comprising Homobifunctional maleimide crosslinkers, di-halide, 1,2-Bis(bromomomethyl)benzene, 1,2-Bis(chloromomethyl)benzene, 1,3-Bis(bromomomethyl)benzene, 1,3-Bis(chloromomethyl)benzene, 1,4-Bis(bromomomethyl)benzene, 1,4-Bis(chloromomethyl)benzene, 3,3′-bis-bromomethyl-biphenyl, or 2,2′-bis-bromomethyl-biphenyl. Particular haloacetyl crosslinkers contain an iodoacetyl or a bromoacetyl group. These homo bifunctional linkers may contain spacers comprising PEG or an aliphatic chain. In particular embodiments, the linker is a bifunctional linker (e.g., di-acid, di-amine, dihalide, N-Hydroxy succinamine (NHS)-activated diesters, bis-maleimides, which may be capable of linking two monomer subunits through amine, ester, thioether, di-thio, or ether bonds.

In certain embodiments, the linker is selected from the group consisting of DIG, PEG4, PEG4-biotin, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, ADA, Boc-IDA, Glutaric acid, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, 1,2-phenylenediacetic acid, Triazine, Boc-Triazine, IDA-biotin, PEG4-Biotin, AADA, aliphatics, aromatics, heteroaromatics, and polyethylene glycol based linkers having a molecular weight from approximately 400 Da to approximately 40,000 Da. In particular embodiments, the linker is a bifunctional linker (e.g., di-acid, di-amine, dihalide, N-Hydroxy succinamine (NHS)-activated diesters, bis-maleimides, which may be capable of linking two monomer subunits through amine, ester, thioether, di-thio, or ether bonds. Non-limiting examples of suitable linker moieties are provided in Table 2.

In particular embodiments, any of the peptide dimer compounds described herein e.g., peptide dimer compounds according to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J), Formula (II), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H), comprise two monomer subunits that are linked by any of the linkers described herein; and any of the peptide monomer compounds described herein, e.g., peptide monomer compounds according to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I and IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D) comprise any of the linkers described herein.

TABLE 2 Illustrative Linker Moieties Abbreviation Description Structure DIG DIGlycolic acid,

PEG4 Bifunctional PEG linker with 4 PolyEthylene Glycol units

PEG13 Bifunctional PEG linker with 13 PolyEthylene Glycol units

PEG25 Bifunctional PEG linker with 25 PolyEthylene Glycol units

PEG1K Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 1000Da PEG2K Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 2000Da PEG3.4K Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 3400Da PEG5K Bifunctional PEG linker with PolyEthylene Glycol Mol wt of 5000Da IDA β-Ala-Iminodiacetic acid

Boc-IDA Boc-β-Ala-Iminodiacetic acid

Ac-IDA Ac-β-Ala-Iminodiacetic acid

IDA-Palm Palmityl-β-Ala-Iminodiacetic acid

GTA Glutaric acid

PMA Pemilic acid

AZA Azelaic acid

DDA Dodecanedioic acid

IPA Isopthalic aicd

1,3-PDA 1,3-Phenylenediacetic acid

1,4-PDA 1,4-Phenylenediacetic acid

1,2-PDA 1,2-Phenylenediacetic acid

Triazine Amino propyl Triazine di-acid

Boc-Triazine Boc-Triazine di-acid

ADA Amino diacetic acid

AADA n-Acetyl amino acetic acid

PEG4-Biotin PEG4-Biotin (Product number 10199, QuantaBioDesign)

1,4 BMB 1,4-Bis(halo-momethyl)benzene

  X = Cl, Br 1,2 BMB 1,2-Bis(halo-momethyl)benzene

  X—Cl, Br 1,3 BMB 1,3-Bis(halo-momethyl)benzene

  X = Cl, Br 1,3 BMBip 3,3′-Bis-Halomethyl-Biphenyl

  X = Cl, Br IDA-Biotin N-Biotin-β-Ala-Iminodiacetic acid

2,2 BMBip 2,2′-Bis-Halomethyl-Biphenyl

  X = Cl, Br BMal Bis-Mal-dPEG

  n = 1 to 20

When the linker is IDA, ADA or any linker with a free amine, it can be acylated, e.g. with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid, straight chain aliphatic acids with 10 to 20 carbon units, cholic acid and other bile acids. In some instances, small PEG (PEG4-PEG13), Glu, IsoGlu or Asp is used as spacer before acylations. It is understood that once bound to a linker or another amino acid, an amino acid reisdue of the peptide compound may undergo structural changes, e.g., an acid may become an amide. Reference to a particular amino acid residue encompasses the amino acid residue in any altered structural form upon binding to a linker or forming an intramolecular bond with another amino acid of the peptide compound.

Aspects of the present invention relate to various peptide monomer compounds that form cyclized structures through a disulfide bond, lactam bond, olefin bond, triazole bond, selenoether bond or diselenide bond. The cyclized structure of each peptide monomer has been shown to increase potency and selectivity of the molecules.

In particular embodiments, the peptide monomer compounds and peptide dimer compounds (also referred to herein collectively as “the peptide compounds”) of the instant invention may comprise one or more terminal modifying groups. In certain embodiments, a terminal end of a peptide compound is modified to include a terminal modifying group selected from the non-limiting group consisting of DIG, PEG4, PEG13, PEG25, PEG1K, PEG2K, PEG4K, PEG5K, Polyethylene glycol having molecular weight from 400 Da to 40,000 Da, IDA, ADA, Glutaric acid, Succinic acid, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, 1,2-phenylenediacetic acid, AADA, and aliphatics, aromatics, and heteroaromatics. In certain embodiments the N- or C-terminus of the peptide compound is linked to a modifying group. In certain embodiments, the N-terminus of a peptide compound is modified by one to three suitable groups, e.g., as represented by Xaa¹, Xaa², and Xaa³, e.g., of Formula (I) or (I-A). The N-terminus may further be acylated. In some instances, the N-terminus further comprises a linker moiety or other modifying group. Similarly, in certain embodiments, the C-terminus of a peptide is modified by a suitable group. For example, the C-terminus may be acylated. In some instances, the C-terminus further comprises a linker moiety, such as but not limited to any of those disclosed herein. In certain embodiments, the C-terminus comprises NH₂ or OH.

The present invention further includes various peptide monomer compounds and peptide dimer compound having peptides that have been substituted with various modified amino acids. For example, some peptides include Tic, Phe(2-carbamoyl), Phe(3-carbamoyl), Phe(4-COOH), Phe(4-OMe), Phe(4-tBu), Homo-Phe, Aic, Cit, Glu(OMe), Dab, Dap, Pen, Sar, Cit, Cav, homoLeu, 2-Nal, D-1-Nal, D-2-Nal, Bip, O-Me-Tyr, β-homoTrp, β-homoPhe, β-homoGlu Phe(4-CF₃), 2-2-Indane, 1-1-Indane, Cyclobutyl, Gla, Phe(4-NH₂), homoPhe, 1-Nal, Nle, homo amino acids, D-amino acids, 3-3-diPhe, cyclobutyl-Ala, HCha, Bip, β-Glu, Phe(4-guanidino), Phe(4-carbomyl) and various N-methylated amino acids. Additional non-limiting examples of non-natural amino acids contemplated by the present invention are shown in Table 1. One having skill in the art will appreciate that additional substitutions may be made to achieve similar desired results, and that such substitutions are within the teaching and spirit of the present invention.

In one aspect, the present invention provides a peptide dimer compound comprising two linked subunits of Formula (I):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴   (Formula (I))

or a pharmaceutically acceptable salt thereof,

wherein one or both subunits of the peptide dimer compound comprises a disulfide bond, a lactam bond, an olefin bond, a triazole bond, a selenoether bond, or a diselenide bond between Xaa⁴ and Xaa¹⁰, and further wherein Formula (I) represents a monomer subunit of a dimer molecule, the monomer subunits are linked to form the peptide dimer compound, and wherein:

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid; Xaa⁴ is any amino acid capable of forming a bond with Xaa¹⁰; Xaa⁵ is selected from the group consisting of: N-Me-Arg, Arg, N-Me-Lys, Phe(4-guanidinoguanidino), Phe(4-carbomyl), Cit, Phe(4-NH₂), N-Me-homoArg, homoArg, Tyr, Dap, Dab, Arg-Me-sym, Arg-Me-asym, Cav, and His;

Xaa⁶ is Ser, Gly, Thr or Ile; Xaa⁷ is Asp, D-Asp, Asp(OMe) or N-Me-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu, Gln, Ser, Asp, Pro, Gly, His, Ala, Phe, Lys, Arg, Asn, Glu, Tyr, Trp, Met, Nle, and N-methyl amino acids, including N-Me-Thr; Xaa⁹ is selected from the group consisting of: Gln, Ser, Asp, Pro, Gly, Ala, Phe, Glu, Ile, Val, N-butyl Ala, N-pental Ala, N-hexyl Ala, cyclobutyl Ala, cyclopentylAla, Leu, Nle, Cba, homoLeu, Cpa, Aoc, and N-Me-Leu; Xaa¹⁰ is any amino acid capable of forming a bond with Xaa⁴; Xaa¹¹ is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, and Tic; Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, Aic, Gln, Cit, Glu(OMe), Asn, D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-Tyr, D-Lys, D-Ile, D-His, N-Me-Glu, N-Me-Asp, alpha-homoGlu, Biphenyl-Gly, Biphenyl-Ala, Homo-Phe, D-1-Nal, D-2-Nal, Thr, and Val, and corresponding D-amino acids and isosteres; Xaa¹³ is absent or Pro or any amino acid; and Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp.

In certain embodiments of Formula (I), Xaa⁷ is Asp, D-Asp, or N-Me-Asp. In certain embodiments of Formula (I), Xaa⁷ is Asp, Asp(OMe) or N-Me-Asp. In certain embodiments, Xaa⁷ is Asp or N-Me-Asp. In certain embodiments, Xaa⁷ is Asp.

In certain embodiments of Formula (I), Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), Phe(4-tBu), Phe(4-CF₃), Phe(3-CF₃), Phe(CF₃), homo-Phe, D-Phe, Phe(2,3-di-Cl), Phe(3,4-di-Cl), N-Me-Tyr, N-Me-Phe, Phe(4-F), Phe(3-F), Phe(4-Me), Phe(3-Me), Phe(2-Me), Phe(3,4-di-Me), Phe(2,4-di-Phe), beta-MethylPhe, and biphenyl-Ala.

In particular embodiments of Formula (I), Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), Asn, D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-Tyr, D-Lys, D-Ile, D-His, N-Me-Glu, N-Me-Asp, alpha-homoGlu, Biphenyl-Gly, Biphenyl-Ala, Homo-Phe, D-1-Nal, D-2-Nal, Thr, and Val.

In particular embodiments of Formula (I), Xaa¹² is selected from the group consisting of aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, and corresponding D-amino acids and isosteres.

In particular embodiments of Formula (I), Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, homoLys, D-Dap, D-Dab, D-Orn, Cys, homoCys, Pen, D-homoCys, D-Cys, and D-Pen.

In particular embodiments of Formula (I), Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, homoLys, D-Dap, D-Dab, Cys, homoCys, Pen, and D-Om.

In one embodiment of Formula (I), Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer.

In another embodiment of Formula (I), Xaa¹⁴ is selected from the group consisting of: Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp.

In particular embodiments of Formula (I), the two C-terminal amino acids of each subunit of a peptide dimer compound possess acid functionality, and they are linked through retroinverse linking by a diamine linker.

In particular embodiments of Formula (I), Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-homoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, and Val; or Xaa¹³ is Pro.

In particular embodiments of Formula (I), Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-homoArg. In particular embodiments of Formula (I), Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val. In particular embodiments of Formula (I), Xaa⁹ is selected from the group consisting of: Cba, homoLeu, and Cpa. In particular embodiments of Formula (I), Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu). In particular embodiments of Formula (I), Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, and Val. In particular embodiments of Formula (I), Xaa¹³ is Pro.

In particular embodiments of Formula (I), Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), Phe(4-tBu), Phe(4-CF₃), Phe(3-CF₃), Phe(CF₃), homo-Phe, D-Phe, Phe(2,3-di-Cl), Phe(3,4-di-Cl), N-Me-Tyr, N-Me-Phe, Phe(4-F), Phe(3-F), Phe(4-Me), Phe(3-Me), Phe(2-Me), Phe(3,4-di-Me), Phe(2,4-di-Phe), beta-MethylPhe, or biphenyl-Ala.

In particular embodiments of Formula (I), Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), Asn, D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-Tyr, D-Lys, D-Ile, D-His, N-Me-Glu, N-Me-Asp, alpha-homoGlu, Biphenyl-Gly, Biphenyl-Ala, Homo-Phe, D-1-Nal, D-2-Nal, Thr, and Val.

In particular embodiments of Formula (I), Xaa⁷ is Asp, D-Asp or N-Me-Asp; Xaa⁹ is selected from the group consisting of: Gln, Ser, Asp, Pro, Gly, Ala, Phe, Glu, Ile, Val, N-butyl Ala, N-pental Ala, N-hexyl Ala, cyclobutyl Ala, Leu, Nle, Cba, homoLeu, Aoc, and N-Me-Leu; Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, and corresponding D-amino acids and isosteres; Xaa¹³ is absent or Pro; and Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, and Pen.

In particular embodiments of Formula (I), Xaa⁷ is Asp, Asp(OMe) or N-Me-Asp.

In certain embodiments, the amino acid directly C-terminal to Xaa¹⁰ is selected from aromatic amino acids, substituted aromatic amino acids, and Tic. In certain embodiments, the amino acid directly C-terminal to Xaa¹⁰ is an aromatic amino acid. In certain embodiments wherein the compound is a peptide dimer, Xaa¹⁴ is Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, homoLys, D-Dap, D-Dab, or D-Om. In certain embodiments, Xaa¹⁴ is Cys, homoCys, or Pen. In certain embodiments, Xaa¹⁴ or the C-terminus comprises an NH₂ or an OH.

In certain embodiments, a free amine in the C-terminal amino acid is capped, e.g., with an acetyl group.

In certain embodiments of any of the formulas described herein, Xaa¹, Xaa² or Xaa³ can only be Ac when located at the N-terminus of the peptide compound, e.g., bound to the N-terminal amino acid of the peptide compound. In particular embodiments of any of the compounds of any of the various formulas described herein, Xaa¹ is Ac, and Xaa² and Xaa³ are both absent or any amino acid.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are amino acid residues capable of binding to each other. Amino acids capable of binding to each other are known in the art, and various examples of specific amino acid residues that bind to each other and the bonds formed are described herein. In particular embodiments, Xaa⁴ and Xaa¹⁰ are capable of binding each other via a covalent bond. In certain embodiments, the covalent bond occurs through side chain groups on Xaa⁴ and Xaa¹⁰. In particular embodiments, the bond is a disulfide bond.

In certain embodiments of any one of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, and I-I), one or both peptide dimer subunit(s) comprises an intramolecular bond between Xaa⁴ and Xaa¹⁰. In certain embodiments of any one of Formula (II) (including II-A), Formula (III), Formula (A), Formula (B), Formula (C), or Formula (D), one or both peptide dimer subunit(s) comprises an intramolecular bond between Xaa¹ and Xaa⁷. In certain embodiments, the bond is a disulfide bond, a lactam bond, an olefin bond, a triazole, a selenoether, or a diselenide bond. In certain embodiments, the bond occurs directly between the two amino acid residues.

In certain embodiments of Formula (I), Xaa⁴ is selected from the group consisting of: Cys, Pen, HomoCys, D-Cys, D-Pen, D-HomoCys, Asp, Glu, HomoGlu, β-Asp, β-Glu, Lys, HomoLys, Om, Dap, Dap, 2-allylglycine, 2-(3′-butenyl)glycine, 2-(4′-pentenyl)glycine, or 2-(5′-hexenyl)glycine, corresponding D-amino acids and sutiable isosteres, and Xaa¹⁰ is selected from the group consisting of: Cys, Asp, Lys, Glu, Pen, HomoAsp, HomoGlu, HomoCys, D-Cys, D-Pen, HomoLys, Om, β-Asp, β-Glu, Dap, Dab, D-HomoCys, 2-allylglycine, 2-(3′-butenyl)glycine, 2-(4′-pentenyl)glycine, or 2-(5′-hexenyl)glycine, corresponding D-amino acids and suitable isosteres.

In certain embodiments of Formula (I), a peptide subunit comprises a disulfide bond between Xaa⁴ and Xaa¹⁰, and Xaa⁴ and Xaa¹⁰ are each selected from the group consisting of: Cys and Pen. In certain embodiments, both Xaa⁴ and Xaa¹⁰ are Pen.

In certain embodiments of Formula (I), Xaa¹⁰ is selected from the group consisting of Asp, homoAsp, Glu, and homoGlu, homoLys, and Xaa⁴ is selected from the group consisting of Lys, Dap, Dab, homoLys, Om, and homoGlu. In certain embodiments, Xaa¹⁰ is selected from the group consisting of Lys, Dap, Dab, homoLys, Om, and homoGlu, and Xaa⁴ is selected from the group consisting of Asp, homoAsp, Glu, homoGlu, and homoLys.

In certain embodiments of Formula (I), Xaa⁴ is selected from the group consisting of Asp, homoAsp, Glu, homoGlu, andhomoLys, Xaa¹⁰ is selected from the group consisting of Lys, Dap, Dab, homoLys, Om, and HGlu, and Xaa⁴ and Xaa¹⁰ are cyclized through an amide bond.

In certain embodiments of Formula (I) wherein a peptide subunit comprises an olefin bond between Xaa⁴ and Xaa¹⁰, Xaa⁴ and Xaa¹⁰ are each selected from the group consisting of: 2-allylglycine, 2-(3′-butenyl)glycine, 2-(4′-pentenyl)glycine, or 2-(5′-hexenyl)glycine, and the peptide is cyclized via ring closing methasis to give the corresponding olefin/“stapled peptide.”

In certain embodiments of Formula (I), Xaa⁴ is Cys, Pen, homoCys, D-Pen, D-Cys or D-homoCys. In certain embodiments, Xaa¹⁰ is Cys, Pen, homoCys, D-Pen, D-Cys or D-homoCys.

In certain embodiments of Formula (I), Xaa⁴ and Xaa¹⁰ are each β-azido-Ala-OH or propargylglycine, and the peptide dimer subunit(s) is cyclized through click chemistry leading to a triazole ring.

In particular embodiments of Formula (I), the intramolecular bond is a disulfide bond or a lactam bond.

In some embodiments, the N-terminal or C-terminal amino acids of both peptide monomer subunits of a peptide dimer, e.g., Xaa¹, Xaa², Xaa³, Xaa¹¹, Xaa¹², Xaa¹³ or Xaa¹⁴, are modified with a suitable linker moiety to form a homo- or hetero-dimer molecule, wherein Formula (I) comprises a dimer formed from two subunits joined by a suitable C- or N-terminal linker.

In one aspect, the present invention provides a peptide dimer compound comprising two linked subunits of Formula (I′):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴   (Formula I′)

or a pharmaceutically acceptable salt thereof, wherein:

Xaa¹ is absent, Ac, or any amino acid;

Xaa² is absent, Ac, or any amino acid;

Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is any amino acid capable of forming a bond with Xaa¹⁰;

Xaa⁵ is selected from the group consisting of: N-Me-Arg, Arg, N-Me-Lys, Phe(4-guanidino), Phe(4-carbomyl), Cit, Phe(4-NH₂), N-Me-homoArg, homoArg, Tyr, Dap, Dab, Arg-Me-sym, Arg-Me-asym, Phe(4-guanidino), Cav, and His;

Xaa⁶ is Ser, Gly, Thr, or Ile;

Xaa⁷ is Asp or D-Asp, Asp(OMe), or N-Me-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu, HomoLeu, Gln, Ser, Asp, Pro, Gly, His, Ala, Phe, Lys, Arg, Asn, Glu, Tyr, Trp, Met, Nle, and N-methyl amino acids, including N-Me-Thr;

Xaa⁹ is selected from the group consisting of: Gln, Ser, Asp, Pro, Gly, Ala, Phe, Glu, Ile, Val, N-butyl Ala, N-pentyl Ala, N-hexyl Ala, cyclobutyl Ala, cyclopentylAla, Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is any amino acid capable of forming a bond with Xaa⁴;

Xaa¹¹ is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids and Tic;

Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, and corresponding D-amino acids and suitable isosteres;

Xaa¹³ is absent or Pro; and

Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, homoLys, D-Dap, D-Dab, Cys, homoCys, Pen, and D-Orn.

In particular embodiments of peptide dimer compounds comprising peptide monomer subunits of Formula (I′), Xaa⁵ and Xaa¹⁰ are linked via an intramolecular bond, e.g., a disulfide bond, a lactam bond, an olefin bond, a triazole bond, a selenoether bond, or a diselenide bond.

In certain embodiments of Formula (I′), Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-homoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro.

In various embodiments, any of the further limitations described for Formula (I) may be present in Formula (I′). Reference throughout to embodiments of Formula (I) also apply to any alternative embodiments of Formula (I) and also to Formula I.

In one aspect, the present invention provides a peptide dimer compound comprising two linked subunits of Formula (II):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰   (Formula (II)

or a pharmaceutically acceptable salt thereof,

wherein one or both subunits of the peptide dimer compound comprises a disulfide bond, a lactam bond, an olefin bond, a triazole bond, a selenoether bond, or a diselenide bond between Xaa¹ and Xaa⁷, and further wherein Formula (II) represents a monomer subunit of a dimer molecule, the monomer subunits are linked to form a dimer molecule in accordance with the present invention, and wherein Xaa¹-Xaa¹⁰ of Formula (II) correspond to Xaa⁴-Xaa¹³ of Formula (I).

In particular embodiments of Formula (II), Xaa¹ and Xaa⁷ are both Cys or Pen; in particular embodiments, both Xaa¹ and Xaa⁷ are Pen.

In particular embodiments of Formula (II), Xaa¹⁰ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer.

In particular embodiments of Formula (II), Xaa¹⁰ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, Pen, D-HomoCys, D-Cys, and D-Pen.

In certain embodiments of Formula (II), Xaa² is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-homoArg; Xaa⁵ is selected from the group consisting of Leu, HomoLeu, Nle and Val; Xaa⁶ is selected from the group consisting of: Cba, HomoLeu, and Cpa; Xaa⁸ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa⁹ is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹⁰ is Pro. In certain embodiments of Formula (II), Xaa² is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-homoArg. In certain embodiments of Formula (II), Xaa⁵ is selected from the group consisting of Leu, HomoLeu, Nle and Val. In certain embodiments of Formula (II), Xaa⁶ is selected from the group consisting of: Cba, HomoLeu, and Cpa. In certain embodiments of Formula (II), Xaa⁸ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu). In certain embodiments of Formula (II), Xaa⁹ is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val. In certain embodiments of Formula (II), Xaa¹⁰ is Pro.

In particular embodiments, one or both subunit of Formula (I) and Formula (II) comprises a disulfide bond, a lactam bond, an olefin bond, a triazole bond, a selenoether bond, or a diselenide bond between Xaa⁴ and Xaa¹⁰ of Formula (I), or Xaa¹ and Xaa⁷ of Formula (II). In particular embodiments, the intramolecular bond is a disulfide bond or a lactam bond. In certain embodiments, a peptide dimer comprises one or more monomer subunits selected from of any one of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J).

In one embodiment of Formula (I), herein referred to as Formula (I-A),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen;

Xaa⁵ is selected from the group consisting of: Arg, N-Me-Arg, Arg, N-Me-Lys, Phe(4-guanidino), Phe(4-carbomylamino), Cit, Phe(4-NH₂), N-Me-HomoArg, HomoArg, Tyr and His;

Xaa⁶ is Ser, Ile, Gly or Thr; Xaa⁷ is Asp, D-Asp or N-Me-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu, Nle, and Val; Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, HomoLeu, Ile, cyclobutyl Ala, cyclopentylAla, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is absent or selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-diPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Phe(2-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Ser, Arg, and Thr; Xaa¹² is absent or selected from the group consisting of Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, D-Asp, Gla, beta-homoGlu, corresponding D-amino acid, any aromatic amino acid, and isosteres thereof, Xaa¹³ is absent or any amino acid; and Xaa¹⁴ is selected from the group consisting of: any amino acid with a free amino group on a side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, or D-Om.

In certain embodiments of Formula (I-A), Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In certain embodiments of Formula (I-A), Xaa⁷ is Asp or N-Me-Asp.

In one embodiment of Formula (I), herein referred to as Formula (I-B),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu and Nle; Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-diPhenylGly, 3,3-diPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Ser, Arg, and Thr; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, corresponding D-amino acid and isosteres thereof; Xaa¹³ is absent or any amino acid; and Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, and D-Orn.

In certain embodiments of Formula (I-B), Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In certain embodiments of Formula (I-B), Xaa⁷ is Asp.

In one embodiment of Formula (I), herein referred to as Formula (I-C),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu and Nle; Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, HomoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenyl Ala, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), HomoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Ser, Arg, and Thr; Xaa¹² is selected from the group consisting of: Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, corresponding D-amino acid and any aromatic amino acid and corresponding isosteres thereof; Xaa¹³ is absent or is any amino acid; and Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, and D-Orn.

In certain embodiments of Formula (I-C), Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In certain embodiments of Formula (I-C), Xaa⁷ is Asp.

In one embodiment of Formula (I), herein referred to as Formula (I-D),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val;

Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃). Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, b-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), HomoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Ser, Arg, and Thr; Xaa¹² is absent or selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, corresponding D-amino acid and isosteres thereof; Xaa¹³ is absent; and Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, and D-Orn.

In certain embodiments of Formula (I-D), Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In certain embodiments of Formula (I-D), Xaa⁷ is Asp.

In one embodiment of Formula (I), herein referred to as Formula (I-E),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val;

Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃). Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Ser, Arg, and Thr; Xaa¹² is absent or selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, or D-Orn.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfidebond.

In certain embodiments of Formula (I-E), Xaa⁷ is Asp.

In one embodiment of Formula (I), herein referred to as Formula (I-F),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3 diPhenyl Ala, Tic, b-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-Carbomyl), Tyr(Me), HomoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, Dihydro Trp, Ile, Leu, Ser, Arg, and Thr; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, beta-homoGlu, corresponding D-amino acid, and isosteres thereof; Xaa¹³ is absent; and Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, and D-Orm.

In certain embodiments of Formula (I-F), Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, and D-N-Me-Lys.

In certain embodiments of Formula (I-F), Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide or a lactam bond.

In certain embodiments of Formula (I-F), Xaa⁷ is Asp.

In one embodiment of Formula (I), herein referred to as Formula (I-G),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Ser, Arg, and Thr Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, or D-Orm.

In certain embodiments of Formula (I-G), Xaa¹⁴ is selected from the group consisting of: D-Lys, N-Me-Lys, and D-N-Me-Lys.

In certain embodiments of Formula (I-G), Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In certain embodiments of Formula (I-G), Xaa⁷ is Asp.

In one embodiment of Formula (I), herein referred to as Formula (I-H),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, b-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), HomoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Ser, Arg, and Thr; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is selected from the group consisting of: D-Lys, N-Me-Lys, and D-N-Me-Lys.

In certain embodiments of Formula (I-H), Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In one embodiment of Formula (I), herein referred to as Formula (I-I),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), and homoPhe; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is selected from the group consisting of: D-Lys, N-Me-Lys, and D-N-Me-Lys.

In certain embodiments of Formula (I-I), Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In certain embodiments of Formula (I-I), Xaa⁷ is Asp.

In one embodiment of Formula (I), herein referred to as Formula (I-J),

Xaa¹ is absent, Ac or any amino acid; Xaa² is absent, Ac or any amino acid; Xaa³ is absent, Ac or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp; Xaa⁸ is Thr; Xaa⁹ is Leu; Xaa¹⁰ is Pen; Xaa¹¹ is Phe(4-tBu)

Xaa¹² is beta-homoGlu; Xaa¹³ is absent;

and Xaa¹⁴ is D-Lys.

In particular embodiments, of Formula (I-J), Xaa⁴ and Xaa¹⁰ are linked via a disulfide bond, and the two monomer subunits are linked via a linker. In particular embodiments, they are linked via their respective C-termini. In one embodiment, the linker is DIG.

In certain embodiments of any one of Formulas (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I), or (I-J), Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, and D-N-Me-Lys.

In certain embodiments of any one of Formulas (II), (III), (A), (B), or (C), Xaa¹⁰ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, and D-N-Me-Lys.

In certain embodiments of any one of Formulas (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I), or (I-J), Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, and D-N-Me-Lys.

In alternative embodiments of any one of Formulas (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I), or (I-J), Xaa¹⁴ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Orn, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In other alternative embodiments, Xaa¹⁴ is selected from the group consisting of: Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In particular embodiments, of these alternatives of Formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I), or (I-J), the two C-terminal amino acids of each subunit of a peptide dimer compound possess acid functionality, and they are linked through retroinverse linking by a diamine linker.

In alternative embodiments of any one of Formulas (II), (III), (A), (B), or (C), Xaa¹⁰ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Orn, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In other alternative embodiments, Xaa¹⁰ is selected from the group consisting of: Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In particular embodiments of these alternatives of Formulas (II), (III), (A), (B), or (C), the two C-terminal amino acids of each subunit of a peptide dimer compound possess acid functionality, and they are linked through retroinverse linking by a diamine linker.

In other embodiments, the present invention includes peptide dimers comprising two peptide subunits of any one of Formulas (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I), or (I-J), but wherein one or both of the Pen residues at Xaa⁴ and Xaa¹⁰ are substituted with Cys. In particular embodiments, both Pen residues at Xaa⁴ and Xaa¹⁰ are substituted with Cys. In particular embodiments, one or both subunits comprise a disulfide bond between Xaa⁴ and Xaa¹⁰.

In particular embodiments of any of Formulas (I), (II), (III) (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I), (I-J), (A), (B), (C), (S), or related peptides, the two peptide subunits are linked via their respective C-termini, e.g., via a linker bound to Xaa¹³ or Xaa¹⁴ of each subunit.

In particular embodiments of any of Formulas (I), (II), (III), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I) or (I-J), (A), (B), (C), (S), or related peptides, the two peptide subunits are linked via their respective N-termini, e.g., via a linker bound to Xaa¹, Xaa², or Xaa³ of each subunit.

In particular embodiments of any of Formulas (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I) or (I-J), or related peptides, Xaa¹ is Ac, and Xaa² and Xaa³ are absent or any amino acid. In certain embodiments, Xaa¹ and Xaa² are absent and Xaa³ is Ac.

In particular embodiments of any of Formulas (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I) or (I-J), or related peptides, any one or more of Xaa¹, Xaa², or Xaa³ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, Cys, homoCys, Pen, and D-Orn. In particular embodiments when Xaa¹, Xaa² or Xaa³ are absent, the two monomer subunits of the peptide dimer compounds are linked with α-amine of the N-terminal amino acid. In particular embodiments, the two sununits are linked with side chain amine, thio group or any functionality capable of linking through the linker of amino acid or the α-amine group of Xaa¹, Xaa² or Xaa³. In particular embodiments, Xaa¹, Xaa² or Xaa³ is D-Lys, N-Me-Lys, or D-N-Me-Lys. In particular embodiments, Xaa¹, Xaa² or Xaa³ is D-Lys, N-Me-Lys, or D-N-Me-Lys, and is located at the N-terminus of the peptide. In particular embodiments, both subunits of a peptide dimer compound comprise an Xaa¹, Xaa² or Xaa³ selected from one of these residues, and the two subunits are linked via their respective N-termini.

In particular embodiments of any of Formulas (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I) or (I-J), or related peptides, any one or more of Xaa¹, Xaa², or Xaa³ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In particular embodiments, this residue is located at the N-terminus of the peptide. In certain embodiments, Xaa¹, Xaa² or Xaa³ is selected from the group consisting of: Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In particular embodiments, this residue is located at the N-terminus of the peptide. In particular embodiments, the two N-terminal amino acids of each subunit of a peptide dimer compound possess acid functionality, and they are linked through retroinverse linking by a diamine linker. In particular embodiments, both subunits of a peptide dimer compound comprise an Xaa¹, Xaa² or Xaa³ selected from one of these residues, and the two subunits are linked via their respective N-termini.

In particular embodiments of any of Formulas (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I) or (I-J), or related peptides including monomer subunits thereof, Xaa⁴ and Xaa¹⁰ are Pen, and Xaa⁵ is N-Me-Arg. In further embodiments of any of these formulas or peptide, Xaa⁴ and Xaa¹⁰ are Pen, Xaa⁵ is N-Me-Arg, and Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu).

In certain embodiments of any one of Formulas (II), (III), (A), (B), or (C), Xaa¹⁰ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, and D-N-Me-Lys.

In one embodiment, a peptide dimer compound or peptide monomer compound of the present invention comprises one or more peptide subunits of Formula (A):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰   (Formula (A))

or a pharmaceutically acceptable salt thereof,

wherein

Xaa¹ is Cys or Pen; Xaa² is N-Methyl-Arg; Xaa³ is Ser; Xaa⁴ is Asp; Xaa⁵ is Thr or Val; Xaa⁶ is Leu or Nle; Xaa⁷ is Cys or Pen; Xaa⁸ is Trp, Tic, Bip, 1-Nal, 2-Nal, Phe(4-tBu), Phe, Tyr, or Phe(4-COOH);

Xaa⁹ is Glu, β-homoGlu, or D-Glu, and Xaa¹⁰ is any amino acid,

wherein the peptide molecule comprises a disulfide bond between Xaa¹ and Xaa⁷.

In particular embodiments of Formula (A), Xaa¹⁰ is D-Lys, N-Me-Lys or N-Me-D-Lys. In particular embodiments, Xaa¹ and/or Xaa⁷ are Pen. In certain embodiments of Formula (A), Xaa¹⁰ is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, Cys, homoCys, Pen, and D-Orn.

In certain embodiments, Xaa¹⁰ or the C-terminus of the peptide comprises an NH₂ or an OH.

Embodiments include peptide dimer compounds comprising the following structure:

(Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴)₂-L,

wherein Xaa¹-Xaa¹⁴ are defined as shown herein for any of Formulas (I), including (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I), and (I-J), and wherein L is any linker moiety linking the C-termini of the two monomer subunits. In particular embodiments, L is selected from the group consisting of DIG, bifunctional PEG13, bifunctional PEG25, bifunctional PEG1K, bifunctional PEG2K, bifunctional PEG3.4K, bifunctional PEG4K, bifunctional PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Isovaleric acid, Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, glutaric acid, Azelaic acid, Pimelic acid, Dodecanedioic acid, suitable aliphatics, aromatics, heteroaromatics, and polyethylene glycol based linkers having a molecular weight from approximately 400 Da to approximately 40,000 Da. When the linker is IDA, ADA or any linker with free amine, it can be acylated with acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid, straight chain aliphatic acids with 10 to 20 carbon units, cholic acid and other bile acids. In some instances small PEG (PEG4-PEG13), Glu, IsoGlu or Asp is used as spacer before acylations. In particular embodiments, the linker is a bifunctional linker (e.g., di-acid, di-amine, dihalide, N-Hydroxy succinamine (NHS)-activated diesters, bis-maleimides, which may be capable of linking two monomer subunits through amine, ester, thioether, di-thio, or ether bonds. In particular embodiments, L is selected from the group consisting of DIG, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Isovaleric acid, Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, cyclopropylacetic acid, succinic acid, glutaric acid, Dodecanedioic acid, suitable aliphatics, suitable aromatics, heteroaromatics, and polyethylene glycols having a molecular weight from approximately 400 Da to approximately 40,000 Da. In one embodiment, the linked is DIG. In other embodiments, L is any of the linkers described herein.

Other embodiments include a peptide dimer compound comprising the following structure:

L-(Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴)₂

wherein Xaa¹-Xaa¹⁴ are defined as shown here for any of Formulas (I), including (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-I), and (I-J), and wherein L is selected from the group consisting of DIG, bifunctional PEG13, bifunctional PEG25, bifunctional PEG1K, bifunctional PEG2K, bifunctional PEG3.4K, bifunctional PEG4K, bifunctional PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Isovaleric acid, Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, glutaric acid, Azelaic acid, Pimelic acid, Dodecanedioic acid, suitable aliphatics, aromatics, heteroaromatics, and polyethylene glycol based linkers having a molecular weight from approximately 400 Da to approximately 40,000 Da. When the linker is IDA, ADA or any linker with free amine, it can be acylated with acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid, straight chain aliphatic acids with 10 to 20 carbon units, cholic acid and other bile acids. In some instances small PEG (PEG4-PEG13), Glu, IsoGlu or Asp is used as spacer before acylations. In particular embodiments, the linker is a bifunctional linker (e.g., di-acid, di-amine, dihalide, N-Hydroxy succinamine (NHS)-activated diesters, bis-maleimides, which may be capable of linking two monomer subunits through amine, ester, thioether, di-thio, or ether bonds. In particular embodiments, L is selected from the group consisting of DIG, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Isovaleric acid, Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, cyclopropylacetic acid, succinic acid, glutaric acid, Dodecanedioic acid, suitable aliphatics, suitable aromatics, heteroaromatics, and polyethylene glycols having a molecular weight from approximately 400 Da to approximately 40,000 Da. In one embodiment, the linked is DIG.

Some sequences of the present invention are derived from the general sequences provided in Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, I-J), Formula (II) (including II-A), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D) or Formula (S). For example, the N-terminus of a decapeptide represented by Xaa⁴-Xaa¹³ of Formula (I) or Xaa¹-Xaa¹⁰ of Formula (II) can be modified by one to three suitable groups, as represented by Xaa¹, Xaa², and Xaa³ of Formula (I). The N-terminus may further be acylated. In particular embodiments, the N-terminus may be acylated with an acylating organic compound selected from the group consisting of 2-Methyl-4,4,4-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, Trifluoromethyl butyl, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations. In some instances, the N-terminus further comprises a suitable linker moiety to facilitate linking together two monomer subunits to form an N-terminal dimer molecule.

In certain embodiments of any peptide dimer copound, e.g., wherein the peptide dimer compound is linked via the N-terminus of one or both monomer subunits, the N-terminal amino acid is any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In certain embodiments, the N-terminal amino acid residue of the monomer subunit is an amino acid with an amine side chain, or an amino acid selected from Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, Cys, homoCys, Pen, and D-Om. In particular embodiments, it is D-Lys, N-Me-Lys, or D-N-Me-Lys.

In addition, as described above for any of the various embodiments of Formula (I), Xaa¹, Xaa² and/or Xaa³ may be an amino acid with an amine side chain, or an amino acid selected from Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Om, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In certain embodiments, it is Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, Cys, homoCys, Pen, and D-Orn, and it may participate in the linkage. The residue participating in the linkage may be located at the N-terminus of the peptide monomer, or it may be an internal amino acid, i.e., not the N-terminal or C-terminal amino acid.

The present invention further includes peptide dimer compounds having subunits based on any of the Formulas described herein, e.g., Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Formula (II) (including II-A), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), or Formula (S), wherein the subunits are linked via one or more internal amino acid residue. For example, an internal amino acid residue of one or more subunits could be modified to include an amino acid or derivative, such as an amino acid with an amine side chain, or an amino acid selected from Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, Cys, homoCys, Pen, and D-Om, capable of forming a bond with a linker. In addition, internal amino acid residues of the monomer subunits may be directly linked to each other (or to a linker) to form a peptide dimer compound. For example, internal lysine residues present in each monomer subunit may bind to each other to form a peptide dimer compound.

In some embodiments, Xaa¹, Xaa², and Xaa³ of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J) are absent. In other embodiments, Xaa¹ is absent, and Xaa² and Xaa³ represent suitable groups for modifying the N-terminus of the peptide, e.g., the decapeptide represented by residues Xaa⁴-Xaa¹³ of Formula (I), and residues Xaa¹-Xaa¹⁰ of Formula (II). Further, in some embodiments Xaa¹ and Xaa² of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J) are absent, and Xaa³ of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J) represents a single suitable group for modifying the N-terminus of the decapeptide subunit. In some embodiments, Xaa¹ and Xaa² of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J) are absent, and Xaa³ of Formula (I) is Ac. In some embodiments, the N-terminal amino acid residue of peptide dimers of either Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Formula (II) (including 2-A), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D) or Formula (S) is acylated. In particular embodiments, the N-terminus may be acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations.

Similarly, the C-terminus of the peptide, e.g., the decapeptide represented by Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Formula (II), Formula (III), Formula (A) Formula (B), Formula (C), Formula (D), or Formula (S) can be modified by a suitable group. The C-terminus may further be acylated, e.g., in the context of peptides dimer subunits that are dimerized via their N-terminus or peptide monomer compounds, e.g., as described herein. In particular embodiments, the C-terminus may be acylated, e.g., on an amino acid with a free amine, with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations. In some instances, the C-terminus further comprises a suitable linker moiety to facilitate linking together two monomer subunits to form a C-terminal dimer molecule.

In certain embodiments of the peptides of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Xaa¹¹, Xaa¹² and Xaa¹³ are absent. In other embodiments, Xaa¹² and Xaa¹³ are absent. In other embodiments, Xaa¹³ is absent. In particular embodiments, Xaa¹⁴ is the C-terminal amino acid of the peptide monomer subunit of the peptide dimer. In particular embodiments, Xaa¹⁴ is modified. In certain embodiments, Xaa¹⁴ is Lysine, D-Lysine, N-methyl-Lysine, Dap or Dab. In particular embodiments, Xaa¹⁴ is Dap or Dab. In certain embodiments, Xaa⁴ comprises an NH₂ moiety.

In some embodiments, the N-terminal residue of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Formula (II), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), or Formula (S) further comprises a linker moiety, e.g., one selected from the group consisting of DIG, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Isovaleric acid, Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, cyclopropylacetic acid, succinic acid, glutaric acid, Dodecanedioic acid, suitable aliphatics, suitable aromatics, heteroaromatics, and polyethylene glycols having a molecular weight from approximately 400 Da to approximately 40,000 Da. Further, in some embodiments, any one or more of Xaa¹-Xaa⁴ are acylated. In particular embodiments, any one or more of Xaa¹-Xaa⁴ are acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations.

In certain embodiments where Xaa⁴ and Xaa¹⁰ are both Cys or Pen, the peptide monomer, or each subunit of the peptide dimer, is cyclized though a disulfide bond between Xaa⁴ and Xaa¹⁰. Preferably, in one embodiment Xaa⁴ is Cys. In another embodiment, preferably Xaa⁴ is Pen. In particular embodiments, Xaa⁴ is Pen; in other embodiments, Xaa¹⁰ is Pen; in other embodiments, both Xaa⁴ and Xaa¹⁰ are Pen.

In certain embodiments of any of the formulas described herein, e.g., Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Xaa⁵ is N-Me-Arg. In certain embodiments, Xaa⁶ is Ser. In certain embodiments, Xaa⁷ is Asp. In certain embodiments, Xaa⁸ is Thr. In certain embodiments, Xaa⁹ is Leu. In one embodiment Xaa¹⁰ is Pen. In another embodiment, Xaa¹⁰ is Cys. In particular embodiments, Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe-(4-OMe), Phe(4-tBu), Phe(4-CN), N-Me-Phe, N-Me-Tyr, b-homoTrp, and Pentafluro-Phe. In certain embodiments, Xaa¹¹ is an aromatic amino acid. In particular embodiments, Xaa¹² is Aic. In particular embodiments, Xaa¹³ is Pro, and Xaa¹¹ and/or Xaa¹² are present. In particular embodiments, Xaa¹⁴ is an amino acyl residue selected from the group consisting of natural amino acids, Dap, Dab, Om, D-Orn, N-Me-Om, N-Me-Dap, N-Me-Dab, N-Me Lys, D-Dap, D-Dab, D-Lys, N-Me-D-Lys, suitable isostere replacements, corresponding D-amino acids, and corresponding N-Methyl amino acids. In at least one embodiment, Xaa¹⁴ is the C-terminus. When Xaa¹⁴ is the C-terminus of the subunit, Xaa¹⁴ may be modified to include a linker moiety in accordance with the present invention. Further, in some embodiments Xaa¹⁴ is N(alpha)Methylated. For some embodiments, any of Xaa¹-Xaa⁵, Xaa⁷-Xaa⁹, and Xaa¹¹-Xaa¹² are N(alpha)Methylated. Xaa⁵ may further be Arg-Me-sym or Arg-Me-asym, and Xaa¹¹ may be O-Me-Tyr, N-Me-Lys(Ac), or 4-Me-Phe. In some instances, any of Xaa¹-Xaa⁴, and Xaa¹¹-Xaa¹⁴ are acylated. For example, in some instances one or more residues at positions Xaa¹-Xaa⁴, and Xaa¹¹-Xaa¹⁴ are acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations.

In certain alternative embodiments of peptides of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Xaa¹⁴ is Cys, HomoCys or Pen, instead of the amino acids listed.

In particular embodiments of any of the peptides described herein, including but not limited to those of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J) (or the corresponding residues of Formula (II), (II-A), (III), (A), (B), (C), (D), (S), (X), or (H), Xaa⁵ is selected from the group consisting of N-Me-Ar, Phe(4-guanidino), Phe(4-NH₂), N-Me-HomoArg, HomoArg, Tyr and His; Xaa⁸ is selected from the group consisting of Leu, HomoLeu, Nle and Val; Xaa⁹ is CPA or Aoc; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu) Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro. In particular embodiments of of any of the compounds and genuses described herein, Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-HomoArg; Xaa⁸ is selected from the group consisting of Leu, HomoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, HomoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro.

In some embodiments, the N-terminal residue or C-terminal residue of any of the peptides described herein, e.g., Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J) or Formula (II) (including II-A) or Formula (III), Formula (A), Formula (B), or Formula (C), Formula (D), or Formula (S) further comprises a conjugated moiety, e.g., a linker moiety, including but not limited to any of those described herein. In particular embodiments, the linker is selected from the group consisting of DIG, bifunctional PEG13, bifunctional PEG25, bifunctional PEG1K, bifunctional PEG2K, bifunctional PEG3.4K, bifunctional PEG4K, bifunctional PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Isovaleric acid, Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, glutaric acid, Azelaic acid, Pimelic acid, Dodecanedioic acid, suitable aliphatics, aromatics, heteroaromatics, and polyethylene glycol based linkers having a molecular weight from approximately 400 Da to approximately 40,000 Da. When the linker is IDA, ADA or any linker with free amine, it can be acylated with acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid, straight chain aliphatic acids with 10 to 20 carbon units, cholic acid and other bile acids. In some instances small PEG (PEG4-PEG13), Glu, IsoGlu or Asp is used as spacer before acylations. In particular embodiments, the linker is a bifunctional linker (e.g., di-acid, di-amine, dihalide, N-Hydroxy succinamine (NHS)-activated diesters, bis-maleimides, which may be capable of linking two monomer subunits through amine, ester, thioether, di-thio, or ether bonds.

Some embodiments of the present invention further include a peptide homodimer or heterodimer molecule, wherein each subunit of the dimer molecule comprises, consists essentially of, or consists of an amino acid sequence represented by at least one of the sequences shown in the accompanying figures and tables.

The invention further includes monomer subunits of any of the peptide dimers described herein (which includes the accompanying figures).

In addition, the present invention includes compounds, including peptide dimer compounds, peptide monomer compound, and monmer subunits, comprising, consisting essentially of, or consisting of one or more (e.g., two) of any of the amino acid sequences described herein, e.g., in any of the formulas, or shown in any of the accompanying tables or figures, e.g., without requiring the presence of any N-terminal modification such as Ac or any C-terminal modification such as NH₂.

The present invention further includes any of the compounds described herein having an alternative N-terminal or C-terminal group. For example, those compounds that show an N-terminal Ac group are also encompassed when their N-terminus is either the unaltered N-terminus of an amino acid, or when a different group is present, and those copmounds that show a C-terminal NH₂ group are also encompassed when their C-terminus is either the unaltered C-terminus of an amino acid, or when a different group is present.

Additional embodiments of the present invention include peptide dimer compounds, peptide monomer compounds, and peptides comprising any of the amino acid sequences shown in any of the formulas, tables or figures herein, and which may include one or more additional amino acid residues. In particular embodiments, the monomer subunits of peptide dimer compounds, the peptide monomer compounds, and the peptides comprise from 7 to 35 amino acid residuesm from 7 to 30 amino acid residues, from 7 to 25 amino acid residues, from 7 to 20 amino acid residues, 7 to 19 amino acid residues, 7 to 18 amino acid residues, 7 to 17 amino acid residues, 7 to 16 amino acid residues, 7 to 15 amino acid residues, 7 to 14 amino acid residues, 7 to 13 amino acid residues, or 7 to 12 amino acid residues. In particular embodiments, the invention includes a peptide comprising the amino acid residues shown for SEQ ID Nos: 1-193 of Table 3 or SEQ ID Nos:194-218 of Table 4, wherein the peptide does not necessarily include (but may include) any of the N-terminal or C-terminal modifications, intramolecular bonds, linkers, or other modifications shown therein. In particular embodiments, the peptide comprises an intramolecular bond, e.g., a disulfide bond between two resisdues, e.g., two Pen residues. The invention further includes peptide monomer compounds, peptide dimer compounds, and other compounds comprising a peptide comprising an amino acid sequence described herein.

The invention further includes a method of manufacturing a peptide compound of the present invention, comprising synthesizing a peptide having a sequence as described herein, and introducing an intramolecular bond between two residues of the peptide (or allowing the intramolecular bond to form). In particular embodiments, the method further includes modifying one or both of the C-terminus and N-terminus of the peptide. In further embodiments, the method includes conjugating a linker to the peptide. In related embodiments, the invention includes a method of preparing a peptide dimer compound comprising: (i) synthesizing a peptide having a sequence as described herein, and introducing an intramolecular bond between two residues of the peptide (or allowing the intramolecular bond to form), and conjugating a linker to the peptide; (ii) synthesizing a peptide having a sequence as described herein (e.g., the same sequence as for step (i)), and introducing an intramolecular bond between two residues of the peptide (or allowing the intramolecular bond to form); and (iii) conjugating the peptide of step (i) to the peptide of step (ii) via the linker attached to the peptide of step (i).

In particular embodiments, the present invention includes a polynucleotide encoding any of the peptide sequences disclosed herein. In particular embodiments, the polynucleotide is DNA, RNA, cDNA, or mRNA, including single-stranded, double-stranded polynucleotide forms thereof, and modified forms thereof. In certain embodiments, the incention includes a vector, e.g., an expression vector or gene therapy vector, comprising a polynucleotide encoding any of the peptides described herein. The vector may further include a promoter and/or other regulatory sequences operably linked to the sequence encoding the peptide sequence described herein. The present invention further includes cells comprising an exogenous or introduced peptide or polynucleotide described herein.

In particular embodiments, the present invention includes peptide dimer compounds comprising two linker monomer subunits, each having the following structure of Formula (S):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴-Xaa¹⁵-Xaa¹⁶-Xaa¹⁷   Formula (S)

wherein Xaa¹-Xaa¹³ correspond to the residues defined at those positions in one of the formulas described herein, e.g., any of Formulas (I), (IV) and wherein Xaa¹³ Xaa¹⁴, Xaa¹⁵, Xaa¹⁶ and Xaa¹⁷ are absent or any amino acid, with the proviso that the C-terminal amino acid corresponds to the residues defined for Xaa¹⁴ in the same formula for which Xaa¹-Xaa¹³ were defined. In particular embodiments, Xaa⁴ and Xaa¹⁰ are linked via a disulfide bond, a lactam bond, an olefin bond, a triazole bond, a selenoether bond, or a diselenide bond.

In particular embodiments, the present invention includes peptide dimer compounds comprising two linker monomer subunits, each having the following structure of Formula (S′):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³   Formula (S′)

wherein Xaa¹-Xaa⁹ correspond to the residues defined at those positions in one of the formulas described herein, e.g., any of Formulas (II), (III), A, B, C or D and wherein Xaa¹⁰, Xaa¹¹, Xaa¹², and Xaa¹³ are absent or any amino acid, with the proviso that the C-terminal amino acid corresponds to the residues defined for Xaa¹⁰ in the same formula for which Xaa⁷-Xaa¹⁰ were defined. In particular embodiments, Xaa¹ and Xaa⁷ are linked via a disulfide bond, a lactam bond, an olefin bond, a triazole bond, a selenoether bond, or a diselenide bond.

In certain embodiments, the peptides further comprise one or more modifying group and/or linker. In certain embodiments, one or both of the N- or C-terminus of the peptides is modified. In particular embodiments, the N-terminus is acylated; and in particular embodiments, the C-terminus comprises a free amine, e.g., NH₂. In particular embodiments, the C-terminus comprises an —OH group. In particular embodiments, the peptide comprises an intramolecular linkage between Xaa⁴ and Xaa¹⁰ of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J) (or Xaa¹ and Xaa⁷ in Formula (II), (III), (A), (B), (C), or (D)). The present invention also includes compounds having any of the structures described herein or shown in any of the accompanying figures.

Further, some embodiments of the present invention comprise a peptide homodimer or hetereodimer molecule, wherein each subunit of the dimer molecule is cyclized through a disulfide bond or a lactam bond, and wherein each monomer subunit of the dimer molecule comprises, consists essentially of, or consists of an amino acid sequence represented by at least one of the sequences shown in the accompanying figures and tables.

In certain embodiments, the present invention provides a peptide dimer compound comprising one or two linked subunits of Formula (III):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰(SEQ ID NO: 343)   (Formula (III))

or a pharmaceutically acceptable salt thereof,

wherein each subunit comprises a disulfide bond between Xaa¹ and Xaa⁷, and further wherein Formula (III) represents a monomer subunit of a dimer molecule, wherein the monomer subunits are linked to form a dimer molecule in accordance with the present invention, and wherein:

Xaa¹ is Pen; Xaa² is N-Me-Arg; Xaa³ is Ser; Xaa⁴ is Asp; Xaa⁵ is Thr; Xaa⁶ is Leu; Xaa⁷ is Pen; Xaa⁸ is Trp;

Xaa⁹ is absent or selected from the group consisting of: Glu, D-Glu, f3-homoGlu; and Xaa¹⁰ is selected from the group consisting of D-Lys and N-Me-Lys.

In particular embodiments, Xaa⁹ is present. In particular embodiments of Formula (III), Xaa¹ is acylated. In particular embodiments of Formula (III), Xaa¹⁰ comprises NH₂ or OH. In particular embodiments of dimers of Formula (III), the two monomer subunits are linked via their respective C-termini via a linker moiety, e.g., DIG. In particular embodiments, the peptide dimer compound is a homodimer.

In one embodiment, a peptide monomer compound or a peptide dimer compound of the present invention comprises a peptide molecule of Formula (B):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰(SEQ ID NO: 344)   (Formula (B))

or a pharmaceutically acceptable salt thereof, wherein

Xaa¹ is Cys or Pen; Xaa² is N-methyl-Arg; Xaa³ is Ser; Xaa⁴ is Asp; Xaa⁵ is Thr; Xaa⁶ is Leu or Nle; Xaa⁷ is Cys, Pen or D-Pen; Xaa⁸ is Trp, Tic, Bip, 1-Nal, 2-Nal, Phe(4-tBu), or Phe(4-COOH);

Xaa⁹ is Glu, β-homoGlu, D-Glu, or Glu(OMe); and Xaa¹⁰ is any amino acid,

wherein the peptide molecule comprises a disulfide bond between Xaa¹ and Xaa⁷.

In particular embodiments, of Formula (B), one or both of Xaa¹ and Xaa⁷ are Pen.

In particular embodiments of Formula (B), Xaa¹⁰ is D-Lys or N-Me-Lys.

In particular embodiments, a peptide dimer comprises two monomer subunits of Formula (B). In particular embodiments, the one or both subunits of the dimer comprise an intramolecular bond between Xaa¹ and Xaa⁷, e.g., a disulfide bond.

Illustrative peptide dimer compounds of the present invention are shown in the Examples and accompanying figures. Peptide dimer compounds are generally shown by providing the amino acid sequence of the monomer subunits of the peptide dimer compound in parentheses, followed by a lower case 2, which indicates that the peptide dimer compound comprises two subunits having the depicted amino acid sequence. The linker may also be shown at the C-terminus of the sequence to indicate that the two monomer subunits are linked via their C-termini, or it is shown at the N-terminus of the sequence to indicate that the two monomer subunits are linked via their N-termini.

The present invention further includes peptide monomer subunits having any of the Formula described herein. In certain embodiments, the peptide monomer subunits are bound to a linker.

The peptide dimer and peptide monomer compounds of the present invention may be free acids or they may be pharmaceutically acceptable salts. In particular embodiments, they are acetate salts.

In certain embodiments, the present invention includes peptide dimer compounds, including pharmaceutically acceptable salts thereof, wherein the two monomer subunits are linked via their C-termini, having a structure of Formula (X):

wherein R₁ and R₂ are H or Me;

n is any integer from 2 to 10;

X is CH₂, NHCO, CONH, S—S, C═O, CHOH, S, S═O, NH, or O; and

Y is a linker moiety.

In particular embodiments, the linker moiety, Y, is any of those shown herein, including but not limited to any of those shown below. In particular embodiments, the linker moiety is selected from DIG, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Ac, IDA-Isovaleric acid, ADA Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, Glu, Asp, D-Glu, D-Asp, 1,4-phenylenediacetic acid, Biphenyl diacetic acid, cyclopropylacetic acid, succinic acid, glutaric acid, Dodecanedioic acid, suitable aliphatic diacids, suitable aromatic diacids, heteroaromatics, and polyethylene glycols having a molecular weight from approximately 400 Da to approximately 40,000 Da. In particular embodiments, the linker is a bifunctional linker (e.g., di-acid, di-amine, dihalide, N-Hydroxy succinamine (NHS)-activated diesters, bis-maleimides, which may be capable of linking two monomer subunits through amine, ester, thioether, di-thio, or ether bonds.

In certain embodiments, a peptide dimer compound of Formula (X) has the structure shown below (Compound X).

In particular embodiments, compounds of Formula (X) and Compound X are salt forms. In one embodiment, they are acetate salts.

In certain embodiments, the present invention includes peptide dimer compounds, including pharmaceutically acceptable salts thereof, wherein the two monomer subunits are linked via their N-termini, having a structure of Formula (H):

wherein R₁ and R₂ are H or Me;

n is any integer from 2 to 10;

X is CH₂, NHCO, CONH, S—S, C═O, CHOH, S, S═O, NH, or O;

Y is a linker moiety; and

Z is NHAc, absent or H.

In particular embodiments, the linker moiety is any of those shown herein, including but not limited to those shown below. In particular embodiments, the linker moiety is selected from DIG, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Ac, IDA-Isovaleric acid, ADA Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, Glu, Asp, D-Glu, D-Asp, 1,4-phenylenediacetic acid, Biphenyl diacetic acid, cyclopropylacetic acid, succinic acid, glutaric acid, Dodecanedioic acid, suitable aliphatic diacids, suitable aromatic diacids, heteroaromatics, and polyethylene glycols having a molecular weight from approximately 400 Da to approximately 40,000 Da. In particular embodiments, the linker is a bifunctional linker (e.g., di-acid, di-amine, dihalide, N-Hydroxy succinamine (NHS)-activated diesters, bis-maleimides, which may be capable of linking two monomer subunits through amine, ester, thioether, di-thio, or ether bonds.

In certain embodiments, a peptide dimer compound of Formula (H) has the structure shown below (Compound H):

Embodiments of the invention include pharmaceutically acceptable salt forms of Compound H, e.g., acetate salts of Compound H.

In certain particular embodiments, the present invention includes peptide dimer compounds comprising one or two monomer subunits comprising one of the following amino acid sequences, wherein the monomer subunits of the peptide dimer are linked via their C-terminus:

(SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); (SEQ ID NO: 220) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 221) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys); (SEQ ID NO: 222) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 224) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys); (SEQ ID NO: 225) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 226) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 227) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 228) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 229) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); or (SEQ ID NO: 230) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys),

and wherein there is a disulfide bond between the two Pen residues of the monomer subunits.

In particular embodiments, the peptides of the monomer subunit further comprise an N-terminal Ac and/or a C-terminal NH₂ or OH. In particular embodiments, there is an disulfide bond between the two Pen residues of the monomer subunit.

In certain particular embodiments, the present invention includes peptide dimer compounds comprising one or two monomer subunits comprising one of the following amino acid sequences, wherein the monomer subunits of the peptide dimer are linked via their N-termini or their C-termini:

(SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β- homoGlu); (SEQ ID NO: 275) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4- COOH)-(β-homoGlu); (SEQ ID NO: 281) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu; (SEQ ID NO: 282) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β- homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β- homoGlu); (SEQ ID NO: 284) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu; (SEQ ID NO: 285) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)- (β-homoGlu); (SEQ ID NO: 285) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)- (β-homoGlu); (SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β- homoGlu); (SEQ ID NO: 282) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β- homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β- homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β- homoGlu); (SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β- homoGlu); or (SEQ ID NO: 281) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu, wherein a disulfide bond links the Pen residues within a monomer dimer subunit.

In particular embodiments wherein the monomer subunits are linked via their N-termini, they are linked by a linker that binds to the N-terminal Pen residue of each monomer subunit. In other embodiments where the monomer subunits are linked via their N-termini, the monomer subunits comprise at least one additional N-terminal amino acid, and wherein the N-terminal amino acid of the monomer subunit is linked by a linker to the other monomer subunit. In particular embodiments, the additional N-terminal amino acid is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Orn, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In particular embodiments, the peptides of the monomer subunit further comprise an N-terminal Ac and/or a C-terminal NH₂ or OH.

In one aspect, the present invention provides a peptide monomer compound of Formula (IV):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴   (Formula (IV))

or a pharmaceutically acceptable salt thereof,

wherein the peptide compound comprises a disulfide bond, a lactam bond, an olefin bond, a triazole bond, a selenoether bond, or a diselenide bond between Xaa⁴ and Xaa¹⁰, wherein:

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid; Xaa⁴ is any amino acid capable of forming a bond with Xaa¹⁰; Xaa⁵ is selected from the group consisting of: N-Me-Arg, Arg, N-Me-Lys, Phe(4-guanidino), Phe(4-carbomyl), Cit, Phe(4-NH₂), N-Me-HomoArg, homoArg, Tyr, Dap, Dab, Arg-Me-sym, Arg-Me-asym, Cav, and His;

Xaa⁶ is Ser, Gly, Thr, or Ile; Xaa⁷ is Asp, D-Asp, Asp(OMe), or N-Me-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu, Gln, Ser, Asp, Pro, Gly, His, Ala, Phe, Lys, Arg, Asn, Glu, Tyr, Trp, Met, Nle, and N-methyl amino acids, including N-Me-Thr; Xaa⁹ is selected from the group consisting of: Gin, Ser, Asp, Pro, Gly, Ala, Phe, Glu, Ile, Val, N-butyl Ala, N-pental Ala, N-hexyl Ala, cyclobutyl Ala, cyclopentylAla, Leu, Nle, Cba, homoLeu, Cpa, Aoc, and N-Me-Leu; Xaa¹⁰ is any amino acid capable of forming a bond with Xaa⁴; Xaa¹¹ is absent or selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Phe(2-carbomyl), Tyr(Me), HomoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydro-Trp, Ile, Leu, Arg, Thr, aromatic amino acids, substituted aromatic amino acids, and Tic; Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, Aic, Gln, Cit, Glu(OMe), Asn, D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-Tyr, D-Lys, D-Ile, D-His, N-Me-Glu, N-Me-Asp, alpha-homoGlu, Biphenyl-Gly, Biphenyl-Ala, homoPhe, D-1-Nal, D-2-Nal, Thr, and Val, and corresponding D-amino acids and isosteres; Xaa¹³ is absent, Pro, or any amino acid; and Xaa¹⁴ is any amino acid.

In certain embodiments of Formula (IV), Xaa⁷ is Asp, Asp(OMe), or N-Me-Asp.

In certain embodiments of Formula (IV), Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, and corresponding D-amino acids and isosteres.

In certain embodiments of Formula (IV), Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), Phe(4-tBu), Phe(4-CF₃), Phe(3-CF₃), Phe(CF₃), homo-Phe, D-Phe, Phe(2,3-di-Cl), Phe(3,4-di-Cl), N-Me-Tyr, N-Me-Phe, Phe(4-F), Phe(3-F), Phe(4-Me), Phe(3-Me), Phe(2-Me), Phe(3,4-di-Me), Phe(2,4-di-Phe), beta-MethylPhe, and biphenyl-Ala.

In particular embodiments of Formula (IV), Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), Asn, D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-Tyr, D-Lys, D-Ile, D-His, N-Me-Glu, N-Me-Asp, alpha-homoGlu, Biphenyl-Gly, Biphenyl-Ala, Homo-Phe, D-1-Nal, D-2-Nal, Thr, and Val.

In particular embodiments of Formula (IV), Xaa¹² is selected from the group consisting of aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, and corresponding D-amino acids and isosteres.

In certain embodiments of Formula (IV), Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-HomoArg; Xaa⁸ is selected from the group consisting of Leu, HomoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, HomoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro. In particular embodiments, the intramolecular bond is a disulfide bond.

In particular embodiments of Formula (IV), Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, and corresponding D-amino acids and suitable isosteres; and Xaa¹³ is absent or Pro.

In certain embodiments, the amino acid directly C-terminal to Xaa¹⁰ is selected from aromatic amino acids, substituted aromatic amino acids, and Tic. In certain embodiments, the amino acid directly C-terminal to Xaa¹⁰ is an aromatic amino acid.

In certain embodiments, Xaa¹⁴ or the C-terminal amino acid does not comprise a free amine.

In certain embodiments, Xaa¹⁴ is Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Orn, Dab, Dap, HomoLys, D-Dap, D-Dab, or D-Om.

In certain embodiments, Xaa¹⁴ or the C-terminus comprises an NH₂ or an OH.

In certain embodiments, a free amine in the C-terminal amino acid is capped, e.g., with an acetyl group.

In certain embodiments, the peptide comprises an intramolecular bond between Xaa⁴ and Xaa¹⁰. In certain embodiments, the bond is a disulfide bond, a lactam bond, an olefin bond, a triazole, a selenoether, or a diselenide bond. In certain embodiments, the bond occurs directly between the two amino acid residues.

In certain embodiments, Xaa⁴ is selected from the group consisting of: Cys, Pen, HomoCys, D-Cys, D-Pen, D-HomoCys, Asp, Glu, HomoGlu, β-Asp, β-Glu, Lys, HomoLys, Om, Dap, Dap, 2-allylglycine, 2-(3′-butenyl)glycine, 2-(4′-pentenyl)glycine, or 2-(5′-hexenyl)glycine, corresponding D-amino acids and suitable isosteres, and Xaa¹⁰ is selected from the group consisting of: Cys, Asp, Lys, Glu, Pen, HomoAsp, HomoGlu, D-Cys, D-Pen, HomoLys, Om, β-Asp, β-Glu, Dap, Dab, D-HomoCys, 2-allylglycine, 2-(3′-butenyl)glycine, 2-(4′-pentenyl)glycine, or 2-(5′-hexenyl)glycine, corresponding D-amino acids and suitable isosteres.

In certain embodiments wherein the cyclic peptide comprises a disulfide bond between Xaa⁴ and Xaa¹⁰, Xaa⁴ and Xaa¹⁰ are each selected from the group consisting of: Cys and Pen. In certain embodiments, both Xaa⁴ and Xaa¹⁰ are Pen.

In certain embodiments wherein the cyclic peptide comprises a lactam bond between Xaa⁴ and Xaa¹⁰, Xaa⁴ and Xaa¹⁰ are each selected from the group consisting of: Lys, HomoLys, Om, Dap, Dab, Asp, Glu, HomoGlu, D-Dap, D-Dab, D-Asp, D-Glu or D-Lys. In certain embodiments, Xaa¹⁰ is Lys, HomoLys, Om, Dap or Dab; and Xaa⁴ is Asp, Glu, or HomoGlu. In certain embodiments, Xaa⁴ is Lys, HomoLys, Om, Dap or Dab; and Xaa¹⁰ is Asp, Glu, or HomoGlu.

In certain embodiments wherein the cyclic peptide comprises a lactam bond between Xaa⁴ and Xaa¹⁰, Xaa¹⁰ is selected from the group consisting of Asp, HAsp, Glu, and HGlu, HLys, and Xaa⁴ is selected from the group consisting of Lys, Dap, Dab, HLys, Om, and HGl. In certain embodiments, Xaa¹⁰ is selected from the group consisting of Lys, Dap, Dab, HLys, Om, and HGlu, and Xaa⁴ is selected from the group consisting of Asp, HAsp, Glu, HGlu, and HLys.

In certain embodiments, Xaa⁴ is selected from the group consisting of Asp, HAsp, Glu, HGlu, and Hlys, Xaa¹⁰ is selected from the group consisting of Lys, Dap, Dab, HLys, Om, and HGlu, and Xaa⁴ and Xaa¹⁰ are cyclized through an amide bond.

In certain embodiments wherein the cyclic peptide comprises an olefin bond between Xaa⁴ and Xaa¹⁰, Xaa⁴ and Xaa¹⁰ are each selected from the group consisting of: 2-allylglycine, 2-(3′-butenyl)glycine, 2-(4′-pentenyl)glycine, or 2-(5′-hexenyl)glycine, and the peptide is cyclized via ring closing methasis to give the corresponding olefin/“stapled peptide.”

In certain embodiments, Xaa⁴ is Cys, Pen, or homoCys. In certain embodiments, Xaa⁴ and Xaa¹⁰ are each β-azido-Ala-OH or propargylglycine, and the peptide is cyclized through click chemistry leading to a triazole ring.

In particular embodiments, the intramolecular bond is a disulfide bond or a lactam bond.

In one aspect, the present invention provides a peptide monomer compound of Formula (IV′):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰-Xaa¹¹-Xaa¹²-Xaa¹³-Xaa¹⁴   (Formula (IV′)),

or a pharmaceutically acceptable salt thereof, wherein:

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid; Xaa⁴ is any amino acid capable of forming a bond with Xaa¹⁰; Xaa⁵ is selected from the group consisting of: N-Me-Arg, Arg, N-Me-Lys, Ph (4-guanidino), Phe(4-carbomyl), Cit, Phe(4-NH₂), N-Me-homoArg, homoArg, Tyr Dap, Dab, Arg-Me-sym, Arg-Me-asym, Cav, and His;

Xaa⁶ is Ser Gly, Thr, or Ile; Xaa⁷ is Asp or D-Asp, Asp(OMe), or N-Me-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu, Gln, Ser, Asp, Pro, Gly, His, Ala, Phe, Lys, Arg, Asn, Glu, Tyr, Trp, Met, Nle, and N-methyl amino acids, including N-Me-Thr; Xaa⁹ is selected from the group consisting of: Gln, Ser, Asp, Pro, Gly, Ala, Phe, Glu, Ile, Val, N-butylAla, N-pentylAla, N-hexyl Ala, cyclobutyl Ala, cyclopentyl-Ala, Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu; Xaa¹⁰ is any amino acid capable of forming a bond with Xaa⁴; and Xaa¹¹ is absent or selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, beta-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Phe(2-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, Dihydro Trp, Ile, Leu, Ser, Arg, Thr, aromatic amino acids, substituted aromatic amino acids, and Tic; Xaa¹² is absent or selected from the group consisting of: aromatic amino acids, substituted aromatic amino acids, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, Tic, and corresponding D-amino acids and suitable isosteres; Xaa¹³ is absent or Pro; and Xaa¹⁴ is any amino acid.

In particular embodiments of Formula (IV′), Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-homoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro.

In various embodiments, any of the features or limitations described for Formula (IV) may be present in Formula (IV′).

In one aspect, the present invention provides a peptide compound of Formula (V):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰   (Formula (V))

or a pharmaceutically acceptable salt thereof, wherein the peptide compound comprises a disulfide bond, a lactam bond, an olefin bond, a triazole bond, a selenoether bond, or a diselenide bond between Xaa¹ and Xaa⁷, wherein Xaa¹-Xaa¹⁰ of Formula (V) corresponds to Xaa⁴-Xaa¹³ of Formula (IV).

In certain embodiments of Formula (V), Xaa² is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-homoArg; Xaa⁵ is selected from the group consisting of Leu, HomoLeu, Nle and Val; Xaa⁶ is selected from the group consisting of: Cba, homoLeu, and Cpa; Xaa⁸ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa⁹ is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹⁰ is Pro. In particular embodiments, the intramolecular bond is a disulfide bond or a lactam bond.

In one embodiment of Formula (IV), herein referred to as Formula (IV-A),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen;

Xaa⁵ is selected from the group consisting of: N-Me-Arg, Arg, N-Me-Lys, Phe(4-guanidino), Phe(4-carbomylamino), Cit, Phe(4-NH₂), N-Me-homoArg, homoArg, Tyr and His;

Xaa⁶ is Ser, Gly, Thr, Ile; Xaa⁷ is Asp or D-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu, Nle, and Val; Xaa⁹ is selected from the group consisting of: Ile, cyclobutyl Ala, cyclopentylAla, Leu, Nle, Cpa, homoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is absent or selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Phe(2-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Arg, and Thr; Xaa¹² is absent or selected from the group consisting of: Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, D-Asp, Gla, beta-homoGlu, corresponding D-amino acid, any aromatic amino acid, and isosteres; Xaa¹³ is absent or any amino acid; and Xaa¹⁴ is any amino acid.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In certain embodiments, Xaa⁷ is Asp.

In one embodiment of Formula (IV), herein referred to as Formula (IV-B),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen or Cys; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu and Nle; Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen or Cys;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Arg, Thr, any substituted aromatic amino acid, and corresponding D-amino acids; Xaa¹² is selected from the group consisting of: Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, corresponding D-amino acid and any aromatic amino acid and corresponding isosteres; Xaa¹³ is absent; and Xaa¹⁴ is any amino acid. In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide or a lactam bond.

In particular embodiments, Xaa⁷ is Asp.

In one embodiment of Formula (IV), herein referred to as Formula (IV-C),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser, Gly, Thr, Ile; Xaa⁷ is Asp or D-Asp;

Xaa⁸ is selected from the group consisting of: Thr, Val, Ile, Leu, homoLeu and Nle; Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-Carbomyl), Tyr(Me), HomoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, Dihydro Trp, Ile, Leu, Ser, Arg, and Thr; Xaa¹² is selected from the group consisting of: Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, corresponding D-amino acid and any aromatic amino acid and corresponding isosteres; Xaa¹³ is absent or is any amino acid; and Xaa¹⁴ is any amino acid.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide or a lactam bond.

In particular embodiments, Xaa⁷ is Asp.

In one embodiment of Formula (IV), herein referred to as Formula (IV-D),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val;

Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, HomoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, b-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), HomoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Arg, and Thr; Xaa¹² is absent or selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, homoGlu, Asp, D-Asp, D-homoGlu, Gla, beta-homoGlu, corresponding D-amino acid and isosteres thereof; Xaa¹³ is absent; and Xaa¹⁴ is any amino acid.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In particular embodiments, Xaa⁷ is Asp.

In one embodiment of Formula (IV), herein referred to as Formula (IV-E),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val;

Xaa⁹ is selected from the group consisting of: Leu, Nle, Cpa, Cba, homoLeu, Aoc, and N-Me-Leu;

Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃) Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Arg, and Thr; Xaa¹² is absent or selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is any amino acid.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide or a lactam bond.

In particular embodiments, Xaa⁷ is Asp.

In one embodiment of Formula (IV), herein referred to as Formula (IV-F),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Arg, and Thr; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, beta-homoGlu, and corresponding D-amino acid and isosteres thereof; Xaa¹³ is absent; and Xaa¹⁴ is any amino acid.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide or a lactam bond.

In particular embodiments, Xaa⁷ is Asp.

In one embodiment of Formula (IV), herein referred to as Formula (IV-G),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, b-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), homoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dDihydroTrp, Ile, Leu, Arg, and Thr; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is any amino acid.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide or a lactam bond.

In particular embodiments, Xaa⁷ is Asp.

In one embodiment of Formula (IV), herein referred to as Formula (IV-H),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), HomoPhe, N-Me-Phe, N-Me-Tyr, Ser, Sar, 2,3-dihydroTrp, Ile, Leu, Ser, Arg, or Thr; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is any amino acid.

In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide bond.

In one embodiment of Formula (IV), herein referred to as Formula (IV-I),

Xaa¹ is absent, Ac, or any amino acid; Xaa² is absent, Ac, or any amino acid; Xaa³ is absent, Ac, or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp or D-Asp; Xaa⁸ is Thr or Val; Xaa⁹ is Leu; Xaa¹⁰ is Pen;

Xaa¹¹ is selected from the group consisting of: Trp, Phe, 2-Nal, 1-Nal, Tyr, His, Phe(4-F), Phe(4-CF₃), Phe(4-CH₃), Phe(4-tBu), Bip, Phe(4-COOH), Gly, 3,3-DiPhenylGly, 3,3-DiPhenylAla, Tic, β-homoTrp, D-1-Nal, D-2-Nal, Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-carbomyl), Phe(3-carbomyl), Tyr(Me), and homoPhe; Xaa¹² is selected from the group consisting of: any aromatic amino acid, Glu, D-Glu, and beta-homoGlu; Xaa¹³ is absent; and Xaa¹⁴ is any amino acid. In certain embodiments, Xaa⁴ and Xaa¹⁰ are linked, e.g. via a disulfide or a lactam bond.

In particular embodiments, Xaa⁷ is Asp.

In one embodiment of Formula (IV), herein referred to as Formula (IV-J),

Xaa¹ is absent, Ac or any amino acid; Xaa² is absent, Ac or any amino acid; Xaa³ is absent, Ac or any amino acid;

Xaa⁴ is Pen; Xaa⁵ is N-Me-Arg; Xaa⁶ is Ser; Xaa⁷ is Asp; Xaa⁸ is Thr; Xaa⁹ is Leu; Xaa¹⁰ is Pen; Xaa¹¹ is Phe(4-tBu)

Xaa¹² is beta-homoGlu; Xaa¹³ is absent;

and Xaa¹⁴ is D-Lys.

In particular embodiments of Formula (IV-J), Xaa⁴ and Xaa¹⁰ are linked via a disulfide bond.

In certain embodiments of any one of Formulas (IV-A), (IV-B), (IV-C), (IV-D), (IV-E), (IV-F), (IV-G), (IV-H), (IV-I) or (IV-J), Xaa¹⁴ is selected from the group consisting of: Lys, D-Lys, N-Me-Lys, D-N-Me-Lys.

In one embodiment, a peptide monomer compound or peptide dimer compound of the present invention comprises a peptide molecule of Formula (C):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰(SEQ ID NO: 345)   (Formula (C))

or a pharmaceutically acceptable salt thereof, wherein.

Xaa¹ is Cys or Pen; Xaa² is N-methyl-Arg; Xaa³ is Ser; Xaa⁴ is Asp; Xaa⁵ is Thr or Val; Xaa⁶ is Leu or Nle; Xaa⁷ is Cys or Pen; Xaa⁸ is Trp, Tic, Bip, 1-Nal, 2-Nal, Phe(4-tBu), Phe, Tyr, or Phe(4-COOH);

Xaa⁹ is Glu, β-homoGlu, or D-Glu; and Xaa¹⁰ is any amino acid,

wherein the peptide molecule comprises a disulfide bond between Xaa¹ and Xaa⁷.

In particular embodiments of Formula (C), Xaa¹⁰ is D-Lys, N-Me-Lys or N-Me-D-Lys. In particular embodiments, Xaa¹ and/or Xaa⁷ are Pen.

In certain embodiments, Xaa¹⁰ or the C-terminus of the peptide comprises an NH₂ or an OH.

In certain embodiments, a free amine in the C-terminal amino acid is capped, e.g., with an acetyl group.

Illustrative peptide monomer compounds of the present invention are shown in the Examples and accompanying figures. In certain embodiments, a peptide monomer compound has the structure shown below (Compound U). In particular embodiments, Compound U is a pharmaceutically acceptable salt form. In one embodiment, it is an acetate salt.

Some sequences of the present invention are derived from the general sequences provided in Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J), Formula (V), Formula (A), (Formula (B), Formula (C), or Formula (D). For example, the N-terminus of a decapeptide represented by Xaa⁴-Xaa¹³ of Formula (IV) or Xaa¹-Xaa¹⁰ of Formula (V), (VI), (A), (B), (C), or (D) can be modified by one to three suitable groups, as represented by Xaa¹, Xaa², and Xaa³ of Formula (IV). The N-terminus may further be acylated. In particular embodiments, the N-terminus may be acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations. In some embodiments, Xaa¹, Xaa², and Xaa³ of Formula (IV) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, and I-I) are absent. In other embodiments, Xaa¹ is absent, and Xaa² and Xaa³ represent suitable groups for modifying the N-terminus of the peptide, e.g., the decapeptide represented by residues Xaa⁴-Xaa¹³ of Formula (IV), and residues Xaa¹-Xaa¹⁰ of Formula (V). Further, in some embodiments, Xaa¹ and Xaa² of Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J) are absent, and Xaa³ of Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J) represents a single suitable group for modifying the N-terminus of the decapeptide subunit. In some embodiments, Xaa¹ and Xaa² of Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J) are absent, and Xaa³ of Formula (IV) is Ac. In some embodiments, the N-terminal amino acid residue of the peptide of either Formula (IV), (V), (VI), (A), (B), (C), or (D) is acylated. In particular embodiments, the N-terminus may be acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations.

Similarly, the C-terminus of the peptide, e.g., the peptide represented by Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J), Formula (V), Formula (VI), Formula (A), Formula (B), Formula (C) or Formula (D) can be modified by a suitable group. The C-terminus may further be acylated. In particular embodiments, the C-terminus may be acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations. In certain embodiments of the peptides of Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J, Xaa¹¹, Xaa¹² and Xaa¹³ are absent. In other embodiments, Xaa¹² and Xaa¹³ are absent. In other embodiments, Xaa¹³ is absent. In particular embodiments, Xaa¹⁴ is the C-terminal amino acid of the peptide. In particular embodiments, Xaa¹⁴ is modified. In certain embodiments, Xaa¹⁴ is Lysine, D-Lysine, N-methyl-Lysine, Dap or Dab. In particular embodiments, Xaa¹⁴ is Dap or Dab. In certain embodiments, Xaa¹⁴ comprises an NH₂ moiety.

In some embodiments, any one or more of Xaa¹-Xaa⁴ are acylated. In particular embodiments, any one or more of Xaa¹-Xaa⁴ are acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations.

In certain embodiments where Xaa⁴ and Xaa¹⁰ are both either Cys or Pen, the peptide is cyclized though a disulfide bond or a lactam bond between Xaa⁴ and Xaa¹⁰. Preferably, in one embodiment Xaa⁴ is Cys. In another embodiment, preferably Xaa⁴ is Pen. In particular embodiments, Xaa⁴ is Pen; in other embodiments, Xaa¹⁰ is Pen; in other embodiments, both Xaa⁴ and Xaa¹⁰ are Pen.

In certain embodiments of any of the peptide dimer or monomer compounds described herein, Xaa⁵ is N-Me-Arg. In certain embodiments, Xaa⁶ is Ser. In certain embodiments, Xaa⁷ is Asp. In certain embodiments, Xaa⁸ is Thr. In certain embodiments, Xaa⁹ is Leu. In one embodiment, Xaa¹⁰ is Pen. In another embodiment, Xaa¹⁰ is Cys. In particular embodiments, Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe-(4-OMe), Phe(4-tBu), Phe(4-F), Phe(4-CN), N-Me-Phe, N-Me-Tyr, β-homoTrp, and Pentafluro-Phe. In particular embodiments, Xaa¹² Glu, D-Glu, beta homoGlu, In particular embodiments, Xaa¹³ is Pro, and Xaa¹¹ and/or Xaa¹² are present In particular embodiments, Xaa¹⁴ is an amino acyl residue selected from the group consisting of natural amino acids, Dap, Dab, Om, D-Om, N-Me-Orn, N-Me-Dap, N-Me-Dab, N-Me Lys, D-Dap, D-Dab, D-Lys, N-Me-D-Lys, isostere replacements, corresponding D-amino acids, and corresponding N-Methyl amino acids. In at least one embodiment, Xaa¹⁴ is the C-terminus. When Xaa¹⁴ is the C-terminus of the subunit, Xaa¹⁴ may be modified to include a linker moiety in accordance with the present invention. Further, in some embodiments Xaa¹⁴ is N(alpha)Methylated. For some embodiments, any of Xaa¹-Xaa⁵, Xaa⁷-Xaa⁹, and Xaa¹¹-Xaa¹² are N(alpha)Methylated. Xaa⁵ may further be Arg-Me-sym or Arg-Me-asym, and Xaa¹¹ may be O-Me-Tyr, N-Me-Lys(Ac), or 4-Me-Phe. In some instances, any of Xaa¹-Xaa⁴, and Xaa¹¹-Xaa¹⁴ are acylated. For example, in some instances one or more residues at positions Xaa¹-Xaa⁴, and Xaa¹¹-Xaa¹⁴ are acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations.

In particular embodiments of any of the peptides described herein, including but not limited to those of Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, and IV-I) (or the corresponding residues of Formula (V), (IV-A), (A), (B), (C), or (D), Xaa⁵ is selected from the group consisting of N-Me-Arg, Phe(4-guanidino), Phe(4-NH₂), N-Me-homoArg, homoArg, Tyr and His; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is CPA or Aoc; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro.

In particular embodiments of any of the compounds and genuses described herein, Xaa⁵ is selected from the group consisting of Cit, Phe(4-carbomyl), and N-Me-homoArg; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is selected from the group consisting of: Cba, homoLeu, and Cpa; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro.

In some embodiments, the C-terminal residue of any of the peptides described herein, e.g., Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, and IV-I) or Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D) further comprises a linker moiety selected from the group consisting of DIG, PEG13, PEG25, PEG1K, PEG2K, PEG3.4K, PEG4K, PEG5K, IDA, IDA-Palm, IDA-Boc, IDA-Isovaleric acid, Triazine, Triazine-Boc, Isophthalic acid, 1,3-phenylenediacetic acid, 1,4-phenylenediacetic acid, glutaric acid, Azelaic acid, Pimelic acid, Dodecanedioic acid, suitable aliphatics, aromatics, heteroaromatics, and polyethylene glycol based linkers having a molecular weight from approximately 400 Da to approximately 40,000 Da.

Some embodiments of the present invention further include a peptide monomer, wherein the peptide monomer comprises, consists essentially of, or consists of an amino acid sequence represented by at least one of the sequences shown in the accompanying figures and tables.

In addition, the present invention includes compounds comprising, consisting essentially of, or consisting of any of the amino acid sequences described herein or shown in any of the accompanying figures. In certain embodiments, the peptides further comprise one or more modifying group and/or linker. In certain embodiments, one or both of the N- or C-terminus of the peptides is modified. In particular embodiments, the N-terminus is acylated. In some embodiments, the N-terminus is acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations. In particular embodiments, the C-terminus comprises a free amine, e.g., NH₂. In particular embodiments, the peptide comprises an intramolecular linkage, e.g., between Xaa⁴ and Xaa¹⁰ of Formula (IV) (or Xaa¹ and Xaa⁷ in Formulas (V), (VI), (A), (B), (C), and (D). The present invention also includes compounds having any of the structures described herein or shown in any of the accompanying figures.

In certain embodiments, the present invention provides a peptide of Formula (VI):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰(SEQ ID NO: 346)   (Formula (VI))

or a pharmaceutically acceptable salt thereof, comprising a disulfide bond between Xaa¹ and Xaa⁷, and wherein:

Xaa¹ is Pen; Xaa² is N-Me-Arg; Xaa³ is Ser; Xaa⁴ is Asp; Xaa⁵ is Thr; Xaa⁶ is Leu; Xaa⁷ is Pen; Xaa⁸ is Trp;

Xaa⁹ is absent or selected from the group consisting of: Glu, D-Glu, β-homoGlu; and Xaa¹⁰ is any amino acid.

In particular embodiments, Xaa¹ and Xaa⁷ are linked via a disulfide bond.

In particular embodiments, Xaa¹⁰ is selected from the group consisting of D-Lys, N-Me-Lys, and D-N-Me-Lys.

In particular embodiments, Xaa⁹ is present.

In particular embodiments of Formula (VI), Xaa¹ is acylated. In some embodiments, Xaa¹ is acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are use as spacer for acylations. In particular embodiments of Formula (VI), Xaa¹⁰ comprises NH₂ or OH.

In one embodiment, a peptide monomer compound or a peptide dimer compound of the present invention comprises a peptide molecule of Formula (D):

Xaa¹-Xaa²-Xaa³-Xaa⁴-Xaa⁵-Xaa⁶-Xaa⁷-Xaa⁸-Xaa⁹-Xaa¹⁰(SEQ ID NO: 347)   (Formula (D))

or a pharmaceutically acceptable salt thereof, wherein

Xaa¹ is Cys or Pen; Xaa² is N-methyl-Arg; Xaa³ is Ser; Xaa⁴ is Asp; Xaa⁵ is Thr; Xaa⁶ is Leu or Nle; Xaa⁷ is Cys, Pen or D-Pen; Xaa⁸ is Trp, Tic, Bip, 1-Nal, 2-Nal, Phe(4-tBu), or Phe(4-COOH);

Xaa⁹ is Glu, β-homoGlu, D-Glu, or Glu(OMe); and Xaa¹⁰ is any amino acid,

wherein the peptide molecule comprises a bond between Xaa¹ and Xaa⁷.

In particular embodiments, of Formula (D), one or both of Xaa¹ and Xaa⁷ are Pen.

In particular embodiments of Formula (D), Xaa⁷ is Cys or Pen.

In particular embodiments of Formula (D), Xaa¹⁰ is D-Lys or N-Me-Lys.

In certain embodiments of Formula (D), Xaa¹⁰ or the C-terminus of the peptide comprises an NH₂ or an OH. In certain embodiments, a free amine in the C-terminal amino acid is capped, e.g., with an acetyl group. In particular embodiments of Formula (D), Xaa¹ is acylated. In some embodiments, Xaa¹ is acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations. In particular embodiments of Formula (D), Xaa¹⁰ comprises NH₂ or OH.

In alternative embodiments any of the peptide monomer compounds herein, including peptide monomer compounds of any one of Formula (IV), including (IV-A)-(IV-J), Formula (V), Formula (VI), Formula (C) and Formula (D), the C-terminal amino acid (e.g., Xaa¹⁴ or Xaa¹⁰) is selected from the group consisting of: any amino acid with an amine side chain, Lys, D-Lys, N-Me-Lys, D-N-Me-Lys, Om, Dab, Dap, HomoLys, D-Dap, D-Dab, D-Orn, Cys, HomoCys, Pen, D-HomoCys, D-Cys, D-Pen, Asp, Glu, D-Asp, D-Glu and HomoSer, Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp. In other alternative embodiments of peptide monomer compounds herein, including peptide monomer compounds of any one of Formula (IV), including (IV-A)-(IV-J), Formula (V), Formula (VI), Formula (C) and Formula (D), the C-terminal amino acid (e.g., Xaa¹⁴ or Xaa¹⁰), the C-terminal residue is selected from the group consisting of: Asp, Glu, homoGlu, D-Asp, D-Glu, D-homoGlu, N-Me-Glu, N-Me-Asp, N-Me-D-Glu, and N-Me-D-Asp.

In further embodiments, the present invention includes any of the peptide monomers comprising an amino acid sequence or having a structure shown in the Examples or in any of the accompanying figures. In certain embodiments, these sequences may include different amino acid residues at the positions that form intramolecular bonds, e.g., Xaa⁴ and Xaa¹⁰ of Formula (IV), including any of those described herein to allow the formation of particular types of bonds, e.g., disulfide, lactam, olefin, triazole (e.g., Click chemistry), selenother, or diselenide bonds.

The present invention further comprises peptides comprising or consisting of any of the amino acid sequences described herein, e.g. any of the amino acid sequences shown in the accompanying tables or figures, but absent any linker. In addition it includes such petides having natural N-termini and/or C-termini, N-terminal and/or C-terminal modifications depicted herein, or other N-terminal or C-terminal modifications.

In certain embodiments, Xaa¹⁰ or the C-terminus of the peptide comprises an NH₂ or an OH. In certain embodiments, a free amine in the C-terminal amino acid is capped, e.g., with an acetyl group. In particular embodiments of Formula (B), Xaa¹ is acylated. In some embodiments, Xaa¹ is acylated with an acylating organic compound selected from the group consisting of 2-me-Trifluorobutyl, Trifluoropentyl, Acetyl, Octonyl, Butyl, Pentyl, Hexyl, Palmityl, Lauryl, Oleoyl, and Lauryl, Trifluoromethyl butyric, cyclopentane carboxylic, cyclopropylacetic, 4-fluorobenzoic, 4-fluorophenyl acetic, 3-Phenylpropionic, tetrahedro-2H-pyran-4carboxylic, succinic acid, and glutaric acid. In some instances, small PEG (e.g., PEG4-PEG13) is used as spacer before acylations. In some instances Glu, IsoGlu, or Asp are used as spacer for acylations. In particular embodiments of Formula (B), Xaa¹⁰ comprises NH₂ or OH. In particular embodiments of dimers of Formula (B), the two monomer subunits are linked via their respective C-termini via a linker moiety, e.g., DIG. In various embodiment, the peptide may further comprise one or more linkers or other modifying groups, e.g., attached to the C- and/or N-terminus.

In further embodiments, the present invention includes any of the peptide monomers comprising an amino acid sequence or having a structure shown in any of the Examples and accompanying figures. In certain embodiments, these sequences may include different amino acid residues at the positions that form intramolecular bonds, e.g., Xaa⁴ and Xaa¹⁰ of Formula (IV), inlcuding any of those described herein to allow the formation of particular types of bonds, e.g., disulfide, lactam, olefin, triazole (e.g., Click chemistry), selenother, or diselenide bonds.

In further embodiments, Xaa⁴ is selected from the group consisting of Cys or Pen. In some embodiments, Xaa¹⁰ is selected from the group consisting of Cys or Pen. In particular embodiments, Xaa⁵ is selected from the group consisting of Phe(4-guanidino), Phe(4-NH₂), N-Me-homoArg, homoArg, Tyr and His; Xaa⁸ is selected from the group consisting of Leu, homoLeu, Nle and Val; Xaa⁹ is CPA or Aoc; Xaa¹⁰ is homoCys; Xaa¹¹ is selected from the group consisting of Tic, Phe(2-carbomyl), Phe(3-carbomyl), Phe(4-carbomyl), Phe(4-COOH), Phe(4-OMe), and Phe(4-tBu); Xaa¹² is selected from the group consisting of Aic, Gln, Cit, Glu(OMe), D-His, Tic, Phe(3-COOH), D-Arg, Bip, D-Trp, Phe, D-Phe, D-Val, D-Thr, D-1-Nal, D-2-Nal, Thr, Val; or Xaa¹³ is Pro.

In addition, it is understood that any of the specific features described for any of the compounds or Formulas described herein may be incorporated to any other compound or Formula described herein. In addition, any of the compositions or methods described herein may be practiced using any of the compounds or compounds of any of the Formulas described herein.

In particular embodiments of any of the various formulas described herein, peptides having the same structure or sequence as disclosed in PCT/US2013/064439, PCT/US2014/032391 or PCT/US2014/032392 are excluded.

In certain embodiments, the present invention includes a peptide comprising any of the amino acid sequences present in any of the peptides described herein. In particular embodiments, the present invention includes a peptide comprising or consisting of one of the following amino acid sequences. In particular embodiments, the present invention includes a peptide monomer compound comprising or consisting of one of the following amino acid sequences. In particular embodiments, the present invention includes a peptide dimer compound comprising or consisting of monomer subunits comprising one of the following amino acid sequences:

(SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); (SEQ ID NO: 220) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4-COOH)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 221) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys); (SEQ ID NO: 222) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 224) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys); (SEQ ID NO: 225) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 226) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 227) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 228) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 229) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); or (SEQ ID NO: 230) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys).

In certain embodiments, any of the peptides of the invention comprise 10-35, 10-30, 10-25, 10-20 or 10-15 amino acids. In particular embodiments, the Pen residues within the peptide are linked via a disulfide bond.

In certain embodiments, the present invention includes a peptide monomer compound comprising a peptide comprising any of the following sequences, wherein in certain embodiments the peptide monomer compound further comprises an N-terminal Ac and/or a C-terminal NH₂ or OH.:

(SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu); (SEQ ID NO: 275) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)- (β-homoGlu); (SEQ ID NO: 281) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu; (SEQ ID NO: 282) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β- homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β- homoGlu); (SEQ ID NO: 284) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu; (SEQ ID NO: 285) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)- (β-homoGlu); (SEQ ID NO: 285) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)- (β-homoGlu); (SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu); (SEQ ID NO: 282) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β- homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β- homoGlu); (SEQ ID NO: 283) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β- homoGlu); (SEQ ID NO: 280) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β- homoGlu); or (SEQ ID NO: 281) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu.

In particular embodiments, the Pen residues within a peptide monomer compound are linked via a disulfide bond.

Peptide Structure and Biological Activity

The present invention provides various novel antagonist peptides. These compounds have been tested to more clearly characterize the increased affinity for α4β7 binding, increased selectivity against α4β1, and increased stability in simulated intestinal fluid (SIF). These novel antagonist molecules demonstrate high binding affinity with α4β7, thereby preventing binding between α4β7 and the MAdCAM ligand. Accordingly, these antagonist peptides have shown to be effective in eliminating and/or reducing the inflammation process in various experiments.

The present invention thus provides various monomer and dimer peptide compounds which bind or associate with the α4β7 integrin, in serum and SIF, to disrupt or block binding between α4β7 and the MAdCAM ligand. The various peptide compounds of the invention may be constructed solely of natural amino acids. Alternatively, the peptide compounds may include non-natural amino acids including, but not limited to, modified amino acids. Modified amino acids include natural amino acids which have been chemically modified to include a group, groups, or chemical moiety not naturally present on the amino acid. The peptide compounds of the invention may additionally include D-amino acids. Still further, the peptide compounds of the invention may include amino acid analogs.

In certain embodiments, peptide molecules of the present invention inhibit or reduced binding between between α4β7 and the MAdCAM ligand. In certain embodiments, a peptide of the present invention reduces binding of α4β7 and the MAdCAM ligand by at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, or at least 90% as compared to a negative control peptide. Methods of determining binding are known in the art and include ELISA assays, for example.

In certain embodiments, a peptide molecule of the present invention has an IC50 of <500 nM, <250 nM, <100 nM, <50 nM, <25 nM, <10 nM, <5 nM, <3 nM, or <2 nM, e.g., in binding to α4β7 or inhibiting α4β7 from binding its receptor. Methods of determining activity are known in the art and include any of those described in the accompanying Examples.

Certain peptide dimer compound and peptide monomer compounds, e.g., disulfide-containing dimers and monomers, have been shown to be gastrointestinal stable and provide high levels of specificity and affinity for the α437 integrin. Some embodiments of the present invention provide a peptide monomer compound or peptide dimer compound having a half-life of greater than 60 minutes when exposed to simulated intestinal fluids (SIF). Some implementations further provide a peptide monomer compound or peptide dimer compound having a half-life from approximately 1 minute to approximately 60 minutes in SIF. Some embodiments of the present invention provide a peptide molecule comprising a half-life of greater than 180 minutes when exposed to SIF. Some implementations further provide a peptide molecule comprising a half-life from approximately 60 minutes to approximately 180 minutes in SIF. Similarly, these peptides are stable under reduced conditions and, in certain embodiments, have half-life >120 min when tested in DTT (Dithiothreitol) assay.

In certain embodiments, a peptide monomer or dimer of the present invention has increased stability, increased gastrointestinal stability, increased stability in stimulated intestinal fluid (SIF), or increased stability in simulated gastric fluid (SGF), as compared to a control peptide. In particular embodiments, a control peptide is a peptide having the identical or a highly related amino acid sequence (e.g., >90% sequence identity) as the peptide, but which does not form a cyclized structure, e.g., through a disulfide or lactam bond. In particular embodiments, a control peptide is a peptide having the identical or a highly related amino acid sequence (e.g., >90% sequence identity) as the peptide, but which forms a disulfide bond through two Cys residues (e.g., as opposed to two Pen residues). In particular embodiments, the only difference between the peptide and the control peptide is that the peptide comprises one or more amino acid substitutions that introduce one or more amino acid residues into the peptide, wherein the introduced residue(s) forms a disulfide or lactam bond with another residue in the peptide.

Methods of determining the stability of a peptide are known in the art. In certain embodiments, the stability of a peptide is determined using an SIF assay, an SGF assay, A DTT assay, or a Cys/CysS assay, e.g., as described in the accompanying Examples. In particular embodiments, a peptide of the present invention has a half-life under a given set of conditions (e.g., temperature) of greater than 1 minute, greater than 10 minutes, greater than 20 minutes, greater than 30 minutes, greater than 60 minutes, greater than 90 minutes, greater than 120 minutes, greater than 3 hours, or greater than four hours when exposed to SIF or SGF. In certain embodiments, the temperature is about 25° C., about 4° C., or about 37° C., and the pH is a physiological pH, or a pH about 7.4.

In some embodiments, the half-life is measured in vitro using any suitable method known in the art, e.g., in some embodiments, the stability of a peptide of the present invention is determined by incubating the peptide with pre-warmed human serum (Sigma) at 37° C. Samples are taken at various time points, typically up to 24 hours, and the stability of the sample is analyzed by separating the peptide monomer or dimer from the serum proteins and then analyzing for the presence of the peptide of interest using LC-MS.

In some embodiments, a peptide of the present invention exhibits improved solubility or improved aggregation characteristics as compared to a control peptide. Solubility may be determined via any suitable method known in the art. In some embodiments, suitable methods known in the art for determining solubility include incubating peptides in various buffers (Acetate pH4.0, Acetate pH5.0, Phos/Citrate pH5.0, Phos Citrate pH6.0, Phos pH 6.0, Phos pH 7.0, Phos pH7.5, Strong PBS pH 7.5, Tris pH7.5, Tris pH 8.0, Glycine pH 9.0, Water, Acetic acid (pH 5.0 and other known in the art) and testing for aggregation or solubility using standard techniques. These include, but are not limited to, visual precipitation, dynamic light scattering, Circular Dichroism and fluorescent dyes to measure surface hydrophobicity, and detect aggregation or fibrillation, for example. In some embodiments, improved solubility means the peptide is more soluble in a given liquid than is a control peptide.

In some embodiments, the peptides of the present invention have less degradation (i.e., more degradation stability), e.g., greater than or about 10% less, greater than or about 20% less, greater than or about 30% less, greater than or about 40% less, or greater than or about 50% less degradation than a control peptide. In some embodiments, degradation stability is determined via any suitable method known in the art. In some embodiments, suitable methods known in the art for determining degradation stability include the method described in Hawe et al J Pharm Sci, VOL. 101, NO. 3, 2012, p 895-913, incorporated herein in its entirety. Such methods are in some embodiments used to select potent peptide monomer or dimer molecules with enhanced shelf lives.

In certain embodiments, peptides of the present invention inhibit or reduce α4β7-mediated inflammation. In related embodiments, peptides of the present invention inhibit or reduce α4β7-mediated secretion of one or more cytokines. Methods of determining inhibition of cytokine secretion and inhibition of signaling molecules are known in the art.

In certain embodiments, peptides of the present invention demonstrate increased binding selectivity. In certain instances, peptides of the present invention binds to α4β7 with at least a two-fold, three-fold, five-fold, or ten-fold greater affinity than the peptides bind to α4β1.

In certain embodiments, peptide antagonists show limited systemic exposure and/or GI-restricted localization following oral administration. In particular embodiments, greater than 50%, greater than 60%, greater than 70%, greater than 80%, or greater than 90% of orally administered peptide inhibitor is localized to gastrointestinal organs and tissues. In particular embodiments, blood plasma levels of orally administered peptide inhibitor are less than 20%, less than 10%, less than 5%, less than 2%, less than 1% or less than 0.5% the levels of peptide inhibitor found in the small intestine, colon, or proximal colon.

In certain embodiments, peptide antagonists of the present invention are efficacious in the treatment of colitis, e.g., ulcerative colitis, and have an IC50 for α4β7 of less than 2 nm or less than 1 nM as determined by ELISA or T cell assay, have a half-life of greater than 4 h, greater than 5 h, greater than 6 h, greater than 12 h or greater than 24 h in simulated intestinal fluid (SIF), rat intestingal fluid (RIW), human intestinal fluid (HIF), colonic wash (CW), intestinal mucosal homogenate (IMH), colonic mucosal homogenate (CMH), simulated gastric fluid (SGF), plasma, Hu S9 or RL S9. In particular embodiments, they are stable after 12 h, 24 h, or 48 h incubation in anaerobic cultures of C. difficile, B. fragilis, E. coli, B. bifidum, and L. acidophilus. In particular embodiments, they show no significant antimicrobial activity against intestinal bacteria grown under anaerobic conditions. In particular embodiments, upon oral administration, the peptide antagonists show minimal exposure in plasma/urine, and exhibit approximately equal exposure in the GI of normal and colitis-diseased animals.

α4β7 integrin present on gut-specific homing lymphocytes is a specific and clinically validated target for IBD. The recently approved α4β7 antagonist antibody drug, Entyvio (vedolizumab) has been described as the future front-line targeted therapy because of its combined efficacy and safety. The present invention provides novel, potent, target specific and orally stable peptides against this integrin target, including selective oral peptide antagonists of α4β7 integrin with limited systemic exposure, and which are effective in blocking T cell homing, preventing mucosal damage in murine models of IBD, and engaging the integrin target as assessed by receptor occupancy in blood cells and in the gastrointestinal tissue. Certain peptides antagonists of the present invention, including Peptide X described in the accompanying examples, have comparable potency and selectivity to vedolizumab in a variety of in vitro cell binding assays. However, the peptide antagonists of the present invention, including Peptide X, are distinguished as oral drugs and by their marked drug exposure in the small intestine and colon, with the potential for expanding the population of IBD patients being treated with targeted therapies.

The compounds of the present invention are peptide homo- or heterodimers formed by linking two subunit monomers at their C- or N-termini. Dimerization of the monomer subunits demonstrate increased potency over their non-dimerized, monomer analogs. Some peptide monomer and peptide dimer compounds of the present invention demonstrated further increased potency as a result of substituting various natural amino acyl residues with N-methylated analog residues. Further still, some peptide monomers and dimer compounds of the present invention comprise monomer subunits that undergo independent cyclization, whereby the cyclized structures demonstrate increased stability over their non-cyclized dimer analogs.

Referring now to Tables 3 and 4, charts are provided which include various data illustrating increased stability for various non-limiting peptide molecules in accordance with the instant invention. Simulated Intestinal Fluid (SIF) Stability assays were performed for the majority of the instant peptide molecules. A selective sampling of these results is provided in Tables 3 and 4.

According to the protocols discussed herein, applicant successfully synthesized and purified integrin antagonist peptide monomer molecules and successfully synthesized, purified, and dimerized the majority of the integrin antagonist peptide dimer molecules shown in the accompanying figures and tables. For those peptides wherein data is not shown, it is expected that they will have an IC50<100 nM in α4β7 ELISA or cell adhersion assays.

Further, substitutions at arginine with N-Me-Arg increased half-life substantially in SIF. In some embodiments, substitution of Cys with Penicillamine (Pen) increased stability significantly in simulated intestinal fluids (SIF). The substitution of Cys with Pen also increased stability under reduced conditions (DTT) indicating improved gastric stability.

Referring now to Tables 3 and 4, charts are provided which include various data illustrating increased potency, selectivity and/or stability for various non-limiting sample peptide dimer molecules in accordance with the instant invention. The peptides also demonstrate low efficacy for α4β1 when compared to α4β7, thereby indicating selectivity against α4β7.

Dimerization of the monomer peptides subunits generally demonstrated increased affinity for α4β7 and/or decreased affinity for α4β1 leading to increased selectivity against α4β1, as compared to the monomer disulfide subunit peptides.

Upon C- and N-terminal dimerization, a significant improvement in potency for α4β7 was also frequently observed. In addition, dimerization also lead to either decrease of potency for a4(31 or no significant change in potency leading to increased selectivity for α4β7 in ELISA and cell adhesion assays.

When Arg is replaced with N-Me-Arg, a significant improvement in potency for α4β7 was shown in both ELISA and cell adhesion assays. N(alpha)methylation further demonstrated increased molecular stability. One having skill in the art will appreciate that methylated isosteres of arginine may further demonstrate similar increases in potency and/or stability.

The invention provides a method for stabilizing a peptide dimer compound or peptide monomer compound, the method comprising a step for substituting Xaa⁴ and Xaa¹⁰ with an amino acid residue selected from the group consisting of Cys and Pen, wherein Xaa⁴ and Xaa¹⁰ form a cyclized structure through a disulfide bond.

One embodiment includes a method for stabilizing a peptide dimer compound or peptide monomer compound, by substituting Xaa⁴ and Xaa¹⁰ (or Xaa¹ and Xaa⁷ in Formulas (II), (III), (IV), (V), (VI), (A), (B), (C), or (D)) with compatible amino acid residues that are capable of forming a cyclized structure through at least one of disulfide bond or lactam bond. In certain embodiments, the compatible amino acids are selected from the group consisting of Cys and Pen, and Xaa⁴ and Xaa¹⁰ form a cyclized structure through a disulfide bond. In certain embodiments, Xaa⁴ is selected from the group consisting of Lys, HLys, Orn, Dap, and Dab, Xaa¹⁰ is selected from the group consisting of Asp, Glu, HGlu, β-Asp, and β-Glu, and Xaa⁴ and Xaa¹⁰ are cyclized through a lactam bond.

Certain embodiments include a method for increasing SIF stability of a peptide dimer or peptide monomer compound of the present invention, comprising a step for substituting N-Me-Arg for one or more unmethylated arginine residues. Other embodiments include a method for increasing SIF stability of a peptide monomer compound of the present invention, comprising a step for substituting Pen for one or more cysteine residues.

Further embodiments include method for increasing redox stability of a peptide dimer compound or peptide monomer compound according to the present invention, comprising a step for substituting Pen for one or more cysteine residues.

Methods of Treatment and Pharmaceutical Compositions

As discussed above, integrins are heterodimers that function as cell adhesion molecules. The α4 integrins, α4β1 and α4β7, play essential roles in lymphocyte migration throughout the gastrointestinal tract. They are expressed on most leukocytes, including B and T lymphocytes, monocytes, and dendritic cells, where they mediate cell adhesion via binding to their respective primary ligands, namely vascular cell adhesion molecule (VCAM) and mucosal addressin cell adhesion molecule (MAdCAM). VCAM and MAdCAM differ in binding specificity, in that VCAM binds both α4β1 and α4β7, while MAdCAM is highly specific for α4β7.

Differences in the expression profiles of VCAM and MAdCAM provide the most convincing evidence of their role in inflammatory diseases. Both are constitutively expressed in the gut; however, VCAM expression extends into peripheral organs, while MAdCAM expression is confined to organs of the gastrointestinal tract. In addition, elevated MAdCAM expression in the gut has now been correlated with several gut-associated inflammatory diseases, including Crohn's disease, ulcerative colitis, and hepatitis C.

The compounds of the invention, including but not limited to those specified in the accompanying examples, possess integrin-antagonist activity. In one embodiment, the condition or medical indication comprises at least one of Inflammatory Bowel Disease (IBD) (including adult IBD, pediatric IBD and adolescent IBD), ulcerative colitis, Crohn's disease, Celiac disease (e.g., nontropical Sprue), enteropathy associated with seronegative arthropathies, microscopic colitis, collagenous colitis, eosinophilic gastroenteritis, radiotherapy, chemotherapy, pouchitis resulting after proctocolectomy and ileoanal anastomosis, gastrointestinal cancer, pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, pericholangitis, chronic bronchitis, chronic sinusitis, asthma, primary sclerosing cholangitis, human immunodeficiency virus (HIV) infection in the GI tract, eosinophilic asthma, eosinophilic esophagitis, gastritis, colitis, microscopic colitis, graft versus host disease (GVDH) (including intestinal GVDH), colitis associated with radio- or chemo-therapy, colitis associated with disorders of innate immunity as in leukocyte adhesion deficiency-1, chronic granulomatous disease, glycogen storage disease type 1b, Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, and Wiskott-Aldrich Syndrome, or pouchitis resulting after proctocolectomy and ileoanal anastomosis and various forms of gastrointestinal cancer, osteoporosis, arthritis, multiple sclerosis, chronic pain, weight gain, and depression. In another embodiment, the condition is pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, pericholangitis, chronic bronchitis, chronic sinusitis, asthma or graft versus host disease. In addition, these compounds may be useful in the prevention or reversal of these diseases when used in combination with currently available therapies, medical procedures, and therapeutic agents.

The compounds of the invention may be used in combination with other compositions and procedures for the treatment of disease. Additionally, the compounds of the present invention may be combined with pharmaceutically acceptable excipients, carriers and diluent, and optionally sustained-release matrices, such as biodegradable polymers, to form therapeutic compositions.

In some embodiments, the present invention provides a method for treating an individual afflicted with a condition or indication characterized by integrin binding, wherein the method comprises administering to the individual an integrin antagonist dimer molecule according to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J), Formula (II), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H) or an integrin antagonist monomer molecule according to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I and IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein.

In one embodiment, a method is provided for treating an individual afflicted with a condition or indication characterized by inappropriate trafficking of cells expressing α4β7 to tissues comprising cells expressing MAdCAM, comprising administering to the individual an α4β7-antagonist dimer molecule according to at least one of Formula (I) Formula (II), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H), or an α4β7-antagonist monomer molecule according to at least one of Formula (IV) Formula (V), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, in an amount sufficient to inhibit (partially or fully) the trafficking of cells expressing α4β7 to tissues comprising cells expressing MAdCAM.

In related embodiments, the present invention provides methods for inhibiting adhesion of CD4+ memory T cells to MAdCAM-1 and/or primary leukocytes in blood, comprising providing to a subject in need thereof an effective amount of a peptide dimer compound or peptide monomer compound of the present invention. The present invention further provides methods of selectively inhibiting adhesion of CD4⁺ memory T cells to tissues expressing MAdCAM-1 in the GI tract, or inhibiting infiltration of α4β7+ cells into the small intestine and the colon (e.g., the distal colon), comprising providing to a subject in need thereof an effective amount of a peptide dimer compound or peptide monomer compound of the present invention.

In another embodiment, the present invention provides a method of inhibiting binding of MAdCAM-1 to α4β7 integrin, comprising contacting the MAdCAM-1 with an integrin antagonist of the present invention. Various embodiments of methods of the present invention may be carried out in vitro, ex vivo, or in vivo. In particular embodiments, exposure of the administered peptide antagonist in GI tissues is at least 10-fold, at least 20-fold, at least 50-fold, or at least 100-fold greater than the exposure in the blood.

In further related embodiments, the present invention provides a method for reducing α4β7+ T cells in the GI tract, e.g., in MLN, isolated lymphoid follicles, and/or Peyers Patches, comprising providing to a subject in need thereof an effective amount of a peptide dimer compound or peptide monomer compound of the present invention. In particular embodiments, the method also causes concomitant increases in α4β7+ T cells in the spleen and/or blood.

In a further related embodiment, the present invention provides a method for increasing receptor occupancy of α4β7+ leukocytes, including memory T cells and/or increasing the percentage of circulating α4β7+ memory T cells in blood, comprising providing to a subject in need thereof an effective amount of a peptide dimer compound or peptide monomer compound of the present invention.

In some embodiments, the present invention provides a method whereby a pharmaceutical composition comprising an integrin antagonist dimer molecule according to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J), Formula (II) (including II-A), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), Formula (H), or an integrin antagonist monomer molecule according to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, is administered to a subject as a first treatment. In another embodiment, the method further comprises administering to the subject a second treatment. In another embodiment, the second treatment is administered to the subject before and/or simultaneously with and/or after the pharmaceutical composition is administered to the subject. In other embodiment, the second treatment comprises an anti-inflammatory agent. In another embodiment, the second pharmaceutical composition comprises an agent selected from the group consisting of non-steroidal anti-inflammatory drugs, steroids, and immune modulating agents. In another embodiment, the method comprises administering to the subject a third treatment.

In one embodiment, a method is provided for treating an individual afflicted with a condition or indication characterized by α4β7 integrin binding, wherein the method comprises administering to the individual an effective amount of a peptide dimer compound or peptide monomer compound of the invention, e.g., an α4β7 integrin antagonist dimer molecule containing subunits of Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Formula (II) (including II-A), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H), or any of the compounds described herein. In some instances, an α4β7 integrin antagonist dimer molecule having subunits selected from and corresponding to Formula (I), Formula (II) Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H), or an α4β7 integrin antagonist monomer molecule according to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, and having high specificity for α4β7 is administered to an individual as part of a therapeutic treatment for a condition or indication characterized by α4β7 integrin binding.

Yet another aspect of the present invention provides a composition for treating a subject in need of α4β7-specific antagonist therapy comprising providing to the subject a peptide dimer compound of Formula (I), or any other compound described herein or in the accompanying figures and tables, having high selectivity for α4β7 integrin in combination with a pharmaceutically acceptable carrier.

Yet another aspect of the present invention provides a composition for treating a subject in need of α4β7-specific antagonist therapy comprising providing to the subject a compound of Formula (I), or any other compound described herein or in the accompanying figures and tables, having high selectivity for α4β7 against α4β1 integrins in combination with a pharmaceutically acceptable carrier.

Yet another aspect of the present invention provides a composition for treating a subject in need of α4β7-specific antagonist therapy comprising providing to the subject a compound of Formula (I), or any other compound described herein or in the accompanying figures or tables, having high selectivity for α4β7 against αEβ7 integrins in combination with a pharmaceutically acceptable carrier.

Yet another aspect of the present invention provides a composition for treating a subject in need of α4β7-specific antagonist therapy comprising providing to the subject a compound of Formula (I), or any other compound described herein or in the accompanying figures or tables, having low selectivity for α4β7 against αEβ7 integrins in combination with a pharmaceutically acceptable carrier.

Yet another aspect of the present invention provides a method for treating a subject in need of integrin-antagonist therapy comprising providing to the subject a peptide of Formula (I), or any other compound described herein or in the accompanying figures and tables.

Some embodiments of the present invention further provide a method for treating an individual with an α4β7 integrin antagonist monomer or dimer molecule that is suspended in a sustained-release matrix. A sustained-release matrix, as used herein, is a matrix made of materials, usually polymers, which are degradable by enzymatic or acid-base hydrolysis or by dissolution. Once inserted into the body, the matrix is acted upon by enzymes and body fluids. A sustained-release matrix desirably is chosen from biocompatible materials such as liposomes, polylactides (polylactic acid), polyglycolide (polymer of glycolic acid), polylactide co-glycolide (copolymers of lactic acid and glycolic acid) polyanhydrides, poly(ortho)esters, polypeptides, hyaluronic acid, collagen, chondroitin sulfate, carboxylic acids, fatty acids, phospholipids, polysaccharides, nucleic acids, polyamino acids, amino acids such as phenylalanine, tyrosine, isoleucine, polynucleotides, polyvinyl propylene, polyvinylpyrrolidone and silicone. A preferred biodegradable matrix is a matrix of one of either polylactide, polyglycolide, or polylactide co-glycolide (co-polymers of lactic acid and glycolic acid).

In some aspects, the invention provides a pharmaceutical composition for oral delivery. The various embodiments and monomer and dimer compositions of the instant invention may be prepared for oral administration according to any of the methods, techniques, and/or delivery vehicles described herein. Further, one having skill in the art will appreciate that the monomer and the dimer compositions of the instant invention may be modified or integrated into a system or delivery vehicle that is not disclosed herein, yet is well known in the art and compatible for use in oral delivery of small dimer peptide molecules.

Oral dosage forms or unit doses compatible for use with the monomer or dimer peptides of the present invention may include a mixture of peptide active drug components, and nondrug components or excipients, as well as other non-reusable materials that may be considered either as an ingredient or packaging. Oral compositions may include at least one of a liquid, a solid, and a semi-solid dosage forms. In some embodiments, an oral dosage form is provided comprising an effective amount of dimer peptide having subunits selected from and corresponding to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J), Formula (II) (including II-A), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H) or a monomer peptide selected from and corresponding to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, wherein the dosage form comprises at least one of a pill, a tablet, a capsule, a gel, a paste, a drink, a syrup, ointment, and suppository. In some instances, an oral dosage form is provided that is designed and configured to achieve delayed release of the peptide dimer in the subjects small intestine and/or colon

In one embodiment, an oral pharmaceutical composition according to any of the formulas described herein comprises an enteric coating that is designed to delay release of the peptide in the small intestine. In at least some embodiments, a pharmaceutical composition is provided which comprises a peptide dimer compound having subunits selected from and corresponding to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J), Formula (II) (including II-A), Formula (III), Formula (A), or Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H) or a monomer peptide selected from and corresponding to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, and a protease inhibitor, such as aprotinin, in a delayed release pharmaceutical formulation. In some instances it is preferred that a pharmaceutical composition of the instant invention comprise an enteric coat that is soluble in gastric juice at a pH of about 5.0 or higher. In at least one embodiment, a pharmaceutical composition is provided comprising an enteric coating comprising a polymer having dissociable carboxylic groups, such as derivatives of cellulose, including hydroxypropylmethyl cellulose phthalate, cellulose acetate phthalate and cellulose acetate trimellitate and similar derivatives of cellulose and other carbohydrate polymers.

In one embodiment, a pharmaceutical composition having subunits selected from and corresponding to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I and I-J), Formula (II) (including II-A), Formula (III), Formula (A), or Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H) or a monomer peptide selected from and corresponding to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, is provided in an enteric coating, the enteric coating being designed to protect and release the pharmaceutical composition in a controlled manner within the subjects lower gastrointestinal system, and to avoid systemic side effects. In addition to enteric coatings, the monomer or dimer peptides of the instant invention may be encapsulated, coated, engaged or otherwise associated within any compatible oral drug delivery system or component. For example, in some embodiments a peptide of the present invention is provided in a lipid carrier system comprising at least one of polymeric hydrogels, nanoparticles, microspheres, micelles, and other lipid systems.

To overcome peptide degradation in the small intestine, some implementations of the present invention comprise a hydrogel polymer carrier system in which a peptide monomer or dimer in accordance with the present invention is contained, whereby the hydrogel polymer protect the peptide from proteolysis in the small intestine and/or colon. The peptides of the present invention may further be formulated for compatible use with a carrier system that is designed to increase the dissolution kinetics and enhance intestinal absorption of the peptides. These methods include the use of liposomes, micelles and nanoparticles to increase GI tract permeation of peptides.

Various bioresponsive systems may also be combined with one or more peptide monomers or dimers of the present invention to provide a pharmaceutical agent for oral delivery. In some embodiments, a peptide monomer or dimer of the instant invention is used in combination with a bioresponsive system, such as hydrogels and mucoadhesive polymers with hydrogen bonding groups (e.g., PEG, poly(methacrylic) acid [PMAA], cellulose, Eudragit®, chitosan and alginate) to provide a therapeutic agent for oral administration. Other embodiments include a method for optimizing or prolonging drug residence time for a peptide monomer or dimer disclosed herein, wherein the surface of the peptide monomer or dimer is modified to comprise mucoadhesive properties through hydrogen bonds, polymers with linked mucins or/and hydrophobic interactions. These modified monomer or dimer molecules may demonstrate increase drug residence time within the subject, in accordance with a desired feature of the invention. Moreover, targeted mucoadhesive systems may specifically bind to receptors at the enterocytes and M-cell surfaces, thereby further increasing the uptake of particles containing the dimer peptide.

Other embodiments comprise a method for oral delivery of a dimer peptide having subunits selected from and corresponding to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J), Formula (II) (including II-A), Formula (III), Formula (A), or Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H), or a monomer peptide selected from and corresponding to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I and I-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, wherein the dimer peptide is used in combination with permeation enhancers that promote the transport of the dimer peptides across the intestinal mucosa by increasing paracellular or transcellular permeation. For example, in one embodiment a permeation enhancer is combined with a dimer peptide having subunits selected from and corresponding to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J), Formula (II) (including II-A), Formula (III), Formula (A), or Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H), or a monomer peptide selected from and corresponding to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, wherein the permeation enhancer comprises at least one of a long-chain fatty acid, a bile salt, an amphiphilic surfactant, and a chelating agent. In one embodiment, a permeation enhancer comprising sodium N-[hydroxybenzoyl)amino] caprylate is used to form a weak noncovalent association with the dimer peptide of the instant invention, wherein the permeation enhancer favors membrane transport and further dissociation once reaching the blood circulation. In another embodiment, a peptide dimer of the present invention is conjugated to oligoarginine, thereby increasing cellular penetration of the monomer or dimer peptides into various cell types. Further, in at least one embodiment a noncovalent bond is provided between a monomer or dimer peptide having subunits selected from and corresponding to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, I-J), Formula (II) (including II-A), Formula (III), Formula (A), or Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H), or a monomer peptide selected from and corresponding to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I, and IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D), or any of the compounds described herein, and a permeation enhancer selected from the group consisting of a cyclodextrin (CD) and a dendrimer, wherein the permeation enhancer reduces peptide aggregation and increasing stability and solubility for the peptide molecule.

Particular embodiments include a method for treating a condition in a subject comprising administering a pharmaceutical composition comprising a peptide dimer compound or peptide monomer compound described herein to the subject, wherein the condition is treatable by reducing the activity (partially or fully) of α4β7 in the subject. In certain embodiments, the subject is a human being. In certain embodiments, the condition is an inflammatory condition of the gastrointestinal system.

Other embodiments include a method for treating a human afflicted with a condition that is associated with a biological function α4β7 and comprise administering to the individual a peptide dimer compound or peptide monomer compound described herein in an amount sufficient to inhibit (partially or fully) the biological function of α4β7 in one or more tissues expressing MAdCAM. In one embodiment, the condition is an inflammatory bowel disease. In certain embodiments, the condition is selected from the group consisting of Inflammatory Bowel Disease (IBD) (including adult IBD, pediatric IBD and adolescent IBD), ulcerative colitis, Crohn's disease, Celiac disease (e.g., nontropical Sprue), enteropathy associated with seronegative arthropathies, microscopic colitis, collagenous colitis, eosinophilic gastroenteritis, radiotherapy, chemotherapy, pouchitis resulting after proctocolectomy and ileoanal anastomosis, gastrointestinal cancer, pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, pericholangitis, chronic bronchitis, chronic sinusitis, asthma, primary sclerosing cholangitis, human immunodeficiency virus (HIV) infection in the GI tract, eosinophilic asthma, eosinophilic esophagitis, gastritis, colitis, microscopic colitis, graft versus host disease (GVDH) (including intestinal GVDH), colitis associated with radio- or chemo-therapy, colitis associated with disorders of innate immunity as in leukocyte adhesion deficiency-1, chronic granulomatous disease, glycogen storage disease type 1b, Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, and Wiskott-Aldrich Syndrome, or pouchitis resulting after proctocolectomy and ileoanal anastomosis and various forms of gastrointestinal cancer, osteoporosis, arthritis, multiple sclerosis, chronic pain, weight gain, and depression. In another embodiment, the condition is pancreatitis, insulin-dependent diabetes mellitus, mastitis, cholecystitis, cholangitis, pericholangitis, chronic bronchitis, chronic sinusitis, asthma or graft versus host disease.

In various embodiments of any of the methods of treatment described herein, the peptide dimer compound or peptide monomer compound is administered to the individual by a form of administration selected from the group consisting of oral, intravenous, peritoneal, intradermal, subcutaneous, intramuscular, intrathecal, inhalation, vaporization, nebulization, sublingual, buccal, parenteral, rectal, vaginal, and topical.

In particular embodiments, the α4β7 integrin antagonist molecule comprises an increased half-life. In one embodiment, the increased half-life is at least one day in vitro or in vivo. In further embodiments, the increased half-life is equal to or greater than a period consistent with no more frequent than twice daily dosing in vivo, the α4β7 integrin antagonist peptide dimer compound or peptide monomer compound comprises or is present in a pharmaceutical composition that is administered orally. In certain embodiments, the increased half-life is from approximately 12 hours to greater than 24 in vivo, and the α4β7 integrin antagonist peptide dimer compound or peptide monomer compound comprises or is present in a pharmaceutical composition that is administered parenterally. In certain embodiments, the increased half-life is from approximately 12 hours to greater than 24 hours in vivo, and the α4β7 integrin antagonist peptide monomer compound comprises or is present in a pharmaceutical preparation that is administered topically.

Related embodiments of the invention provide a method for treating an individual in need thereof with an α4β7 integrin antagonist monomer or dimer molecule having an increased half-life. In one aspect, the present invention provides an integrin antagonist monomer or dimer molecule having a half-life of at least several hours to one day in vitro or in vivo (e.g., when administered to a human subject) sufficient for daily (q.d.), twice daily (b.i.d.), or thrice daily (t.i.d.) dosing of a therapeutically effective amount. In another embodiment, the monomer or dimer molecule has a half-life of three days or longer sufficient for weekly (q.w.) dosing of a therapeutically effective amount. Further, in another embodiment the monomer or dimer molecule has a half-life of eight days or longer sufficient for bi-weekly (b.i.w.) or monthly dosing of a therapeutically effective amount. In another embodiment, the monomer or dimer molecule is derivatized or modified such that is has a longer half-life as compared to the underivatized or unmodified dimer molecule. In another embodiment, the monomer or dimer molecule contains one or more chemical modifications to increase serum half-life.

When used in at least one of the treatments or delivery systems described herein, a therapeutically effective amount of one of the compounds of the present invention may be employed in pure form or, where such forms exist, in pharmaceutically acceptable salt form. As used herein, a “therapeutically effective amount” of the compound of the invention is meant to describe a sufficient amount of the peptide monomer or dimer compound to treat an integrin-related disease, (for example, to reduce inflammation associated with IBD) at a desired benefit/risk ratio applicable to any medical treatment. It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular subject will depend upon a variety of factors including: a) the disorder being treated and the severity of the disorder; b) activity of the specific compound employed; c) the specific composition employed, the age, body weight, general health, sex and diet of the subject; d) the time of administration, route of administration, and rate of excretion of the specific compound employed; e) the duration of the treatment; f) drugs used in combination or coincidental with the specific compound employed, and like factors well known in the medical arts. For example, it is well within the skill of the art to start doses of the compound at levels lower than those required to achieve the desired therapeutic effect and to gradually increase the dosage until the desired effect is achieved.

Alternatively, a compound of the present invention may be administered as pharmaceutical compositions containing the compound of interest in combination with one or more pharmaceutically acceptable excipients. A pharmaceutically acceptable carrier or excipient refers to a non-toxic solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. The compositions may be administered parenterally, intracistemally, intravaginally, intraperitoneally, intrarectally, topically (as by powders, ointments, drops, suppository, or transdermal patch), or buccally. The term “parenteral” as used herein refers to modes of administration which include intravenous, intramuscular, intraperitoneal, intrastemal, subcutaneous, intradermal and intraarticular injection and infusion.

Pharmaceutical compositions for parenteral injection comprise pharmaceutically acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, as well as sterile powders for reconstitution into sterile injectable solutions or dispersions just prior to use. Examples of suitable aqueous and nonaqueous carriers, diluents, solvents or vehicles include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), carboxymethylcellulose and suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate. Proper fluidity may be maintained, for example, by the use of coating materials such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.

These compositions may also contain adjuvants such as preservative, wetting agents, emulsifying agents, and dispersing agents. Prevention of the action of microorganisms may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents such as sugars, sodium chloride, and the like. Prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption, such as aluminum monostearate and gelatin.

Injectable depot forms are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide, poly(orthoesters), poly(anhydrides), and (poly)glycols, such as PEG. Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controlled. Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissues.

The injectable formulations may be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium just prior to use.

Topical administration includes administration to the skin or mucosa, including surfaces of the lung and eye. Compositions for topical lung administration, including those for inhalation and intranasal, may involve solutions and suspensions in aqueous and non-aqueous formulations and can be prepared as a dry powder which may be pressurized or non-pressurized. In non-pressurized powder compositions, the active ingredient in finely divided form may be used in admixture with a larger-sized pharmaceutically acceptable inert carrier comprising particles having a size, for example, of up to 100 micrometers in diameter. Suitable inert carriers include sugars such as lactose.

Alternatively, the composition may be pressurized and contain a compressed gas, such as nitrogen or a liquefied gas propellant. The liquefied propellant medium and indeed the total composition is preferably such that the active ingredient does not dissolve therein to any substantial extent. The pressurized composition may also contain a surface active agent, such as a liquid or solid non-ionic surface active agent or may be a solid anionic surface active agent. It is preferred to use the solid anionic surface active agent in the form of a sodium salt.

A further form of topical administration is to the eye. A compound of the invention is delivered in a pharmaceutically acceptable ophthalmic vehicle, such that the compound is maintained in contact with the ocular surface for a sufficient time period to allow the compound to penetrate the corneal and internal regions of the eye, as for example the anterior chamber, posterior chamber, vitreous body, aqueous humor, vitreous humor, cornea, iris/ciliary, lens, choroid/retina and sclera. The pharmaceutically acceptable ophthalmic vehicle may, for example, be an ointment, vegetable oil or an encapsulating material. Alternatively, the compounds of the invention may be injected directly into the vitreous and aqueous humour.

Compositions for rectal or vaginal administration are preferably suppositories which may be prepared by mixing the compounds of this invention with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at room temperature but liquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.

Compounds of the present invention may also be administered in the form of liposomes. As is known in the art, liposomes are generally derived from phospholipids or other lipid substances. Liposomes are formed by mono- or multi-lamellar hydrated liquid crystals that are dispersed in an aqueous medium. Any non-toxic, physiologically acceptable and metabolizable lipid capable of forming liposomes can be used. The present compositions in liposome form can contain, in addition to a compound of the present invention, stabilizers, preservatives, excipients, and the like. The preferred lipids are the phospholipids, including the phosphatidyl cholines (lecithins) and serines, both natural and synthetic. Methods to form liposomes are known in the art.

Total daily dose of the compositions of the invention to be administered to a human or other mammal host in single or divided doses may be in amounts, for example, from 0.0001 to 300 mg/kg body weight daily and more usually 1 to 300 mg/kg body weight.

Non-Invasive Detection of Intestinal Inflammation

The peptides of the invention may be used for detection, assessment and diagnosis of intestinal inflammation by microPET imaging using an orally stable compound described herein, and that is further labeled with at least one of a chelating group and a detectable label as part of a non-invasive diagnostic procedure. In one embodiment, an integrin antagonist monomer or dimer molecule is conjugated with a bifunctional chelator to provide an orally stable monomer or dimer molecule. In another embodiment, an integrin antagonist monomer or dimer molecule is radiolabeled to provide an orally stable monomer or dimer molecule. The orally stable, chelated or radiolabeled monomer or dimer molecule is then administered to a subject orally or rectally. In one embodiment, the orally stable monomer or dimer molecule is included in drinking water. Following uptake of the monomer or dimer molecules, microPET imaging may be used to visualize inflammation throughout the subject's bowels and digestive track.

Methods for Determining Receptor Occupancy and Integrin Expression

The peptides of the invention may be used for determining binding and α4β7 integrin receptor occupancy of a peptide, e.g., on CD4 T cells, naïve CD4 T cells, or B cells. For example, receptor occupancy of blood cells may be determined using blood obtained from a subject (e.g., a mammal or human) having been administered a peptide dimer compound or peptide monomer compound of the present invention, e.g., when the compound was orally administered to the subject. Alternatively, receptor occupancy may be determined based on in vitro binding and competition of a peptide dimer compound or peptide monomer compound of the present invention.

In certain embodiments for FACS analysis, heparinized whole blood from animals *e.g., cyanos) is stained with each of two panels of antibodies to evaluate (1) the extent of α4β7 receptor occupancy in samples treated with a peptide dimer compound or peptide monomer compound described herein; and (2) the abundance of circulating α4β7+, αEβ7+, and α4β7+αEβ7+ lymphocyte subsets. Receptor occupancy and integrin expression are assessed within memory CD4 T cells, naïve CD4 T cells, and B cells. To evaluate receptor occupancy, whole blood samples are first treated with 1 mM MnCl₂ to allow peptide binding, and then pre-incubated+/−1 uM unlabeled peptide to fully occupy (i.e., block) the α4β7 receptor. Blocked and unblocked samples were stained with 1 nM Alexa 647-labeled peptide, followed by staining with antibodies against α4β7, CD45, CD4, CD45RA, and CD19. Samples are processed to lyse erythrocytes and fix leukocytes, followed by staining with a second-step reagent (streptavidin-BV421) and wash steps. To assess integrin expression and cell subset abundance, whole blood samples are stained with antibodies against α4, β7, and αE, in addition to antibodies against CD45, CD4, CD45RA, and CD19. Samples are processed to lyse erythrocytes and fix leukocytes, followed by staining with a second-step reagent (streptavidin-BV421) and wash steps. The stained samples are analyzed by flow cytometry, collecting a constant sample volume to allow calculation of absolute cell counts.

In one embodiment for determining receptor occupancy, a blood sample obtained from a subject having been administered (e.g., orally) a peptide dimer compound or peptide monomer compound of the present invention is incubated with a detectably labeled version of the same peptide dimer compound or peptide monomer compound, under conditions and for a time sufficient to allow binding of the labeled peptide to cells within the blood sample. The samples are then stained with antibodies and/or other reagents that bind to α4β7 integrin, and other markers of CD4 Tcells, naïve CD4 T cells and/or B cells. The samples are then processed to lyse erythrocytes and fix leukoctyes, stained with a second-step reagent, e.g., to allow antibody detection and/or cell sorting, washed, and analyzed by flow cytometry to determine the amount of competitor peptide binding to the CD4 Tcells, naive CD4 T cells and/or B cells. The receptor occupancy of the peptide dimer compound or peptide monomer compound may be determined based upon the amount of labeled peptide detected bound to the cells, optionally further in view of the amount of α4β7 detected on the cells.

In another embodiment for determining receptor occupancy, a blood sample obtained from a donor animal (e.g., a mammal or human not treated with the peptide) is incubated with an unlabeled peptide dimer compound or peptide monomer compound of the present invention, or with a negative control (such as buffer only or an unrelated peptide), under conditions and for a time sufficient to allow binding of the unlabeled peptide to cells within the blood sample. The samples are then stained with a detectably-labeled version of the same peptide dimer compound or peptide monomer compound of the present invention (under conditions and for a time sufficient to allow binding of the labeled peptide to cells within the blood sample), followed by staining with antibodies and/or other reagents that bind to α4β7 integrin, and other markers of CD4 Tcells, naive CD4 T cells and/or B cells. The samples are then processed to lyse erythrocytes and fix leukoctyes, stained with a second-step reagent, e.g., to allow antibody detection and/or cell sorting, washed, and analyzed by flow cytometry to determine the amount of competitor peptide binding to the CD4 Tcells, naive CD4 T cells and/or B cells. The receptor occupancy of the test peptide may be determined based upon the amount of labeled peptide detected bound to the cells, optionally further in view of the amount of α4β7 detected on the cells.

In another embodiment for evaluating receptor occupancy of a test peptide, a blood sample is incubated with an unlabeled test peptide or a negative control (such as buffer only or an unrelated peptide), under conditions and for a time sufficient to allow binding of the test peptide to cells within the blood sample. The samples are then stained with a detectably-labeled peptide dimer compound or peptide monomer compound of the present invention (competitor peptide), followed by staining with antibodies and/or other reagents that bind to α4β7 integrin, and other markers of CD4 Tcells, naive CD4 T cells and/or B cells. The samples are then processed to lyse erythrocytes and fix leukoctyes, stained with a second-step reagent, e.g., to allow antibody detection and/or cell sorting, washed, and analyzed by flow cytometry to determine the amount of competitor peptide binding to the CD4 Tcells, naive CD4 T cells and/or B cells. The receptor occupany of the test peptide may be determined based upon the amount of competitor peptide detected bound to the cells, further in view of the amount of α4β7 detected on the cells.

In one example, whole blood samples (e.g., mouse, rat or human blood) are first treated with 1 mM MnCl2 to allow test peptide binding, and then pre-incubated +/−1 uM unlabeled Peptide X to bind (i.e., block) the α4β7 receptor, or with no peptide or a negative control peptide (unblocked). Blocked and unblocked samples are stained with 1 nM Alexa 647-labeled Peptide X, followed by staining with antibodies against α4β7, CD45, CD4, CD45RA, and CD19. Samples are processed to lyse erythrocytes and fix leukocytes, followed by staining with a second-step reagent (streptavidin-BV421) and wash steps. All stained samples were analyzed by flow cytometry, collecting a constant sample volume to allow calculation of absolute cell counts.

To assess integrin expression and cell subset abundance, whole blood samples are stained with antibodies against α4, β7, and αE, in addition to antibodies against CD45, CD4, CD45RA, and CD19. Samples are processed to lyse erythrocytes and fix leukocytes, followed by staining with a second-step reagent (streptavidin-BV421) and wash steps. All stained samples were analyzed by flow cytometry, collecting a constant sample volume to allow calculation of absolute cell counts.

In particular embodiments, to prevent receptor internalization, cells are kept cold during all steps prior to fization, and incubations are performed at 4 degrees C. (except for red blood cell lysis).

Detailed description of one embodiment of the assay is described below.

MnCl₂ is added to each blood sample (about 100 uL) at a final concentration of about 1 mM; the sample is mixed and incubated at 4 degrees C. for 10-15 minutes.

Unlabeled peptide (or control) is added to the sample at a final concentration of luM or DMSO vehicle control (matching concentration of DMSO) to the appropriate blood samples, mixed, and incubated at 4 degrees C. for 60 minutes.

Labeled peptide is added at a final concentration of InM to the appropriate blood samples mixed, and incubated at 4 degrees C. for 60 minutes.

Antibody staining cocktail is added to each blood sample, e.g., integrin a4/b7/ae cocktail including labeled antibodies that bind CD45 (C45 V500), CD4 (CD4 Ax700), CD45RA (CD45RA FITC), CD19 (C19 PE-CF₅₉₄), integrin α4 (integrin (a4 biotin), integrin J37 (integrin J37 PE), or integrin αE (integrin αE PE-Cy7); or receptor occupancy staining cocktail including CD45 V500, CD4 Ax700, CD45Ra FITc, CD19 PE-CF594, vedolizumab-biotin, and integrin αE PE-Cy7; mixed, and incubated at 4 degrees C. for 30 minutes.

Samples are then treated with a 10-volume excess of 1×FACS Lysing Solution (diluted from 10× stock) to lyse red blod cells, mixed thoroughly, and incubated at Room Temperature for 10 minutes. Samples are centrifuged at 400×g for 5 min, supernatant is removed, and cells are resuspended in PBS/BSA/MnCl2 to wash. Cells are centrifuged again similarly and supernatant removed; washing is repeated.

Cells are stained with Streptavidin BV421 at a final dilution of 1:1000 in PBS/BSA/MnCl₂, mixed thoroughly, and incubated at 4 degrees C. for 30 minutes.

Cells are washed twice with PBS/BSA/MnCl₂ as above, and then resuspended in PBS/BSA/MnCl₂

Samples are run on a flow cytometer, collecting a consistent sample volume across all samples to allow calculation of absolute event counts through FACs analysis. Receptor occupany of the test peptide may be determined based on the relative amount of competitor peptide that binds to unblocked samples as compared to samples blocked with the test peptide.

In another specific example, heparinized whole blood from human donors is stained with each of two panels of antibodies to evaluate (1) the extent of α4β7 receptor occupancy in peptide-treated samples and (2) the abundance of circulating α4β7⁺, αEβ7⁺, and α4β7+αEβ7⁺ lymphocyte subsets. Receptor occupancy and integrin expression are assessed within memory CD4 T cells, naïve CD4 T cells, and B cells.

To evaluate receptor occupancy, whole blood samples are first treated with 1 mM MnCl₂ to allow peptide binding and then pre-incubated +/−1 uM unlabeled peptide to fully occupy (i.e., block) the α4β7 receptor. Blocked and unblocked samples are stained with 1 nM Alexa 647-labeled peptide, followed by staining with antibodies against α4β7, CD45, CD4, CD45RA, and CD19. Samples are then processed to lyse erythrocytes and fix leukocytes, followed by staining with a second-step reagent (streptavidin-BV421) and wash steps.

To assess integrin expression and cell subset abundance, whole blood samples are stained with antibodies against α4, β7, and αE, in addition to antibodies against CD45, CD4, CD45RA, and CD19. Samples are then processed to lyse erythrocytes and fix leukocytes, followed by staining with a second-step reagent (streptavidin-BV421) and wash steps.

All stained samples are analyzed by flow cytometry, collecting a constant sample volume to allow calculation of absolute cell counts. In one, receptor occupancy is determined by determining an amount of labeled peptide that binds to the blood cells after the blood cells have been contacted with unlabeled peptide, and determining an amount of α4β7 present on the cells, wherein the difference between the amount of ^(a)4β7 present on the cells and the amount bound by the labeled peptide represents receptor occupancy by the unlabeled peptide.

In certain embodiments, the present invention includes a labeled (e.g., detectably-labeled) compound or peptide described here, including but not limited to any of the peptide dimer compounds described herein e.g., peptide dimer compounds according to Formula (I) (including any of I-A, I-B, I-C, I-D, I-E, I-F, I-G, I-H, I-I, and I-J), Formula (II), Formula (III), Formula (A), Formula (B), Formula (C), Formula (D), Formula (S), Formula (X), or Formula (H), or any of the peptide monomer compounds described herein, e.g., peptide monomer compounds according to Formula (IV) (including any of IV-A, IV-B, IV-C, IV-D, IV-E, IV-F, IV-G, IV-H, IV-I and IV-J), Formula (V) (including V-A), Formula (VI), Formula (A), Formula (B), Formula (C), or Formula (D). In particular embodiments, the peptide compound or peptide is fluorescently labeled.

In certain embodiments, the present invention includes a detectably labeled peptide, peptide monomer compound or peptide dimer compound of the present invention, comprising any of the amino acid sequences present in any of the peptides described herein. In particular embodiments, the peptide compound or peptide is fluorescently labeled.

In particular embodiments, the present invention includes a peptide, peptide dimer compound, or peptide monomer compound comprising any of the following amino acid sequences:

(SEQ ID NO: 219) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); (SEQ ID NO: 220) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 221) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys); (SEQ ID NO: 222) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 224) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys); (SEQ ID NO: 225) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 226) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 227) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 228) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 223) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 229) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 295) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); or (SEQ ID NO: 230) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys), wherein there is optionally a disulfide bond between the two Pen reisdues.

In particular embodiments, the peptide dimer compound comprises one of the following sequences or structures:

(SEQ ID NO: 296) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)]₂-DIG; (SEQ ID NO: 297) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys)]₂-DIG; (SEQ ID NO: 298) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)]₂-DIG; (SEQ ID NO: 299) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)]₂-DIG; (SEQ ID NO: 300) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)]₂-DIG; (SEQ ID NO: 301) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys)]₂-DIG; (SEQ ID NO: 302) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)]₂-DIG; (SEQ ID NO: 303) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)]₂-DIG; (SEQ ID NO: 304) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)]₂-DIG; (SEQ ID NO: 305) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)]₂-DIG; (SEQ ID NO: 300) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)]₂-DIG; (SEQ ID NO: 306) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)]₂-DIG; (SEQ ID NO: 307) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)]₂-DIG; (SEQ ID NO: 308) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)]₂-DIG; (SEQ ID NO: 213) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 130) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 215) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 137) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 231) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 138) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 218) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 149) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 141) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 232) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 231) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 142) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)-NH₂]₂-DIG; (SEQ ID NO: 213) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 214) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)-NH₂]₂-DIG; (SEQ ID NO: 233) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 234) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 235) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 236) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 237) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 238) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 239) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 240) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 241) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 242) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)-OH₂]₂-DIG; (SEQ ID NO: 237) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-OH]₂-DIG; (SEQ ID NO: 243) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)-OH]₂-DIG; (SEQ ID NO: 309) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-OH]₂-DIG; or (SEQ ID NO: 244) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)-OH]₂-DIG, wherein in certain embodiments, there is a disulfide bond between the two Pen residues.

In particular embodiments, the peptide monomer compound comprises one of the following sequences or structures:

(SEQ ID NO: 310) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); (SEQ ID NO: 311) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 312) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys); (SEQ ID NO: 313) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 314) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 315) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys); (SEQ ID NO: 316) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys); (SEQ ID NO: 317) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 318) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 319) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 314) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys); (SEQ ID NO: 320) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys); (SEQ ID NO: 310) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys); (SEQ ID NO: 321) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys); (SEQ ID NO: 251) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 252) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 253) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)-OH; (SEQ ID NO: 254) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 255) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 256) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys)-OH; (SEQ ID NO: 257) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 258) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)-OH; (SEQ ID NO: 259) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)-OH; (SEQ ID NO: 260) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)-OH; (SEQ ID NO: 255) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 261) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)-OH; (SEQ ID NO: 322) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-OH; (SEQ ID NO: 262) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)-OH; (SEQ ID NO: 263) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 264) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe-(4-COOH)-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 265) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-Lys)-NH₂; (SEQ ID NO: 266) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 267) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 268) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-Glu-(N-Me-Lys)-NH₂; (SEQ ID NO: 153) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 269) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homoGlu)-(N-Me-Lys)-NH₂; (SEQ ID NO: 270) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(N-Me-Lys)-NH₂; (SEQ ID NO: 271) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-2-Nal-(β-homoGlu)-(N-Me-Lys)-NH₂; (SEQ ID NO: 267) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(D-Lys)-NH₂; (SEQ ID NO: 272) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-1-Nal-(β-homoGlu)-(N-Me-Lys)-NH₂; (SEQ ID NO: 323) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-(β-homoGlu)-(D-Lys)-NH₂; or (SEQ ID NO: 273) Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Trp-Glu-(N-Me-D-Lys)-NH₂; wherein in certain embodiments, there is a disulfide bond between the two Pen residues.

In particular embodiments, the peptide, peptide monomer compound, or peptide dimer compound, is labeled, for example, detectably labeled, e.g., fluorescently labeled with a fluorophore or radiolabeled with a radioisotope. A variety of detectable molecules may be used, such as a radioisotopes, fluorochromes, dyes, enzymes, nanoparticles, chemiluminescent markers, biotin, or other monomer known in the art that can be detected directly (e.g., by light emission) or indirectly (e.g., by binding of a fluorescently-labeled antibody).

The use of detectable labels is well known in the art. Detectable labels may be used according to the invention. Methods for conjugating polypeptides and detectable labels are well known in the art, as are methods for imaging using detectable labels. Chimeric polypeptide sensors tagged with a detectable label may be employed in a wide variety of assays, employing a wide variety of labels. In some embodiments of the present invention, detection of a species of ubiquitin protein or ubiquitin like protein can facilitated by attaching a detectable label to the chimeric polypeptide sensor. In some embodiments, detection of a species of ubiquitin protein or species of ubiquitin like protein can be facilitated by attaching a detectable label to a competitor ubiquitin protein or a competitor ubiquitin-like protein.

Examples of detectable labels include but are not limited to radionucleotides, enzymes, coenzymes, fluorescers, chemiluminescers, chromogens, enzyme substrates or co-factors, enzyme inhibitors, prosthetic group complexes, free radicals, particles, dyes, and the like. Several radioisotopes can be used as detectable molecules for labeling peptides including, for example, 32P, 33P, 35S, 3H, and 125I. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, β-galactosidase, or acetylcholinesterase; examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin, coumarin, Alexa488, Oregon green 488, rhodamine green, Alexa 532, Cy3, Bodipy 588/586, Alexa586, TAMRA, Rox, Alexa 594, Texas red, Bodipy 630/650, Cy5, Alexa647, IR Dye 680, IR Dye 680, IR Dye 700 DX, Cy5.5, Alexa 750, IR Dye 800CW, IR Dye 800, Atto 532, Atto 465; an example of a luminescent material is luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin; and examples of suitable radioactive material include 125 I, 131 I, 35 S, or 3 H. In some embodiments, the detectable labels include fluorescent proteins. Suitable fluorescent proteins include TagBFP, mTagBFP2, Azurite, EBFP2, mKalamal, Sirius, Sapphire, T-Sapphire, ECFP, Cerulean, SCFP3A, mnTurquoise, miTurquoise2, monomeric Midoriishi-cyan, TagCFP, mTFP1, GFP, EGFP, Emeral, Superfolder GFP, monomeric Azanmi Green, TagGFP2, mUKG, mWasabi, Clover, mNeonGreen, EYFP, YFP, Citrine, Venus, SYFP2, TagYFP, monomeric Kusabira Orange, MKOK mKO2, mOrange, mOrange2, mRaspberry, mCherry, mStrawberry, mTangerine, tdTomato, TagRFP, TagRFPI, mApple, mRuby, mRuby2, TagRFP675, IFP1.4, iFRP, mKeima Red, LSS-mKate1, LSS-mKate2, mBeRFP, PA-GFP, PAmCherryl, PATagRFP, Kaede green, Kaede red, KikGR1 green, KikGR1 red, PS-CFP2, mEos2 green, mEos2 red, mnEos3.2 green, mEos3.2 red, PSmOrange. In some embodiments of the present invention, detectable labels also include quenchers suitable for fluorescence resonance energy transfer (FRET) pairings. Examples of suitable quenchers include Dabcyl, BHQ1, BHQ2, BHQ3, CY5Q, CY7Q, lowablack FQ, lowablack RQ, IR Dye QC-1, QSY35, QSKY7, QXL570, QXL610, QXL680.

EXAMPLES Example 1 Synthesis of Peptide Molecules

The peptide monomer compounds and peptide dimer compounds of the present invention may be synthesized by many techniques that are known to those skilled in the art. Novel peptide monomer and peptide dimer subunits were synthesized, purified, and dimerized using the techniques provided herein.

Synthesis

The peptides of the present invention were synthesized using the Merrifield solid phase synthesis techniques on Protein Technology's Symphony multiple channel synthesizer using standard Fmoc chemistryThe amino acids used are Fmoc amino acids with a standard side chain protecting group compatible with Fmoc chemistry. The peptides were assembled using HBTU (O-Benzotriazole-N,N,N′,N′-tetramethyl-uronium-hexafluoro-phosphate), Diisopropylethylamine (DIEA) coupling conditions. For some amino acid couplings, PyAOP (7-Azabenzotriazol-1-yloxy)tripyrrnolidinophosponium hexafluorophosphate) and DIEA conditions were used. For some amino acid couplings Oxyma (Ethyl (hydroxyimino)cyanoacetate) and DIC conditions were used. Rink Amide MBHA resin (100-200mesh 0.57 mmol/g) was used for peptides with C-terminal amides and pre-loaded Wang Resin with N-α-Fmoc protected amino acid was used for peptides with C-terminal acids. The coupling reagents (HBTU and DIEA prenmixed) were prepared at 100 mmol concentration. Similarly, amino acids solutions were prepared at 100 mmol concentration.

Assembly

The peptides were assembled using standard Symphony synthesizer protocols for Fmoc chemistry. The peptide sequences were assembled as follows: Resin (250 mg, 0.14 mmol) in each reaction vial was washed twice with 4 ml of DMF followed by treatment with 2.5 ml of 20% 4-methyl piperidine (Fmoc de-protection) for 10 min. The resin was then filtered and washed two times with DMF (4 ml) and re-treated with N-methyl piperifine for an additional 30 minute. The resin was again washed three times with DMF (4 ml) followed by addition of 2.5 ml of amino acid and 2.5 m of HBTU-DIEA mixture. After 45 min of frequent agitations, the resin was filtered and washed three times with DMF (4 ml each). After completing the coupling reaction, the resin was washed three times with DMF (4 m each) before proceeding to the next amino acid coupling. Fmoc deprotection and amino acid coupling cycles were repeated for the specific number of amino acids in the peptide sequence. For Pen (Trt) coupling coupling to the N-Me-Arg, 2.0 eq amino acid, 2.2 eq oxyma, and 2.0 eq DIC was used, and completion of the reaction was monitored using Chloranil test.

Cleavage

Following completion of the peptide assembly, the peptide was cleaved from the resin by treatment with a cleavage reagent, such as reagent K (82.5% trigluoroacetic acid, 5% water, 5% thioanisole, 5% phenol, 2.5% 1,2-ethanedithiol). The cleavage reagent was able to successfully cleave the peptide from the resin, as well as all remaining side chain protecting groups.

The cleaved peptides were precipitated in cold diethyl ether followed by two washings with ethyl ether. The filtrate was poured off and a second aliquot of cold ether was added, and the procedure was repeated. The crude peptide was dissolved in a solution of acetonitrile:water (7:3 with 1% TFA) and filtered. The quality of linear peptide was then verified using electrospray ionization mass spectrometry (ESI-MS) (Micromass/Waters ZQ) before being purified.

Disulfide Bond Formation via Oxidation

50 mg of crude, cleaved peptide was dissolved in 20 ml of water:acetonitrile. Saturated Iodine in acetic acid was then added drop wise with stirring until yellow color persisted. The solution was stirred for 15 minutes, and the reaction was monitored with analytic HPLC and LCMS. When the reaction was completed, solid ascorbic acid was added until the solution became clear. The solvent mixture was then purified by first being diluted with water and then loaded onto a reverse phase HPLC machine (Luna C18 support, 10 u, 100A, Mobile phase A: water containing 0.1% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA, gradient began with 5% B, and changed to 50% B over 60 minutes at a flow rate of 15 ml/min). Fractions containing pure product were then freeze-dried on a lyophilyzer.

Lactam Bond Formation

100 mg of crude, cleaved peptide (approx. 0.12 mmol) was dissolved in 100 ml of anhydrous dichloromethane. HOBt (1-Hydroxybenzotriazole hydrate) (0.24 mmol, 2 equivalents) was added followed by DIEA (N,N-Diisopropylethylamine) (1.2 mmol, 10equivalents) and TBTU (O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate)(0.24 mmol, 2 equivalents). The mixture was stirred overnight and followed the reaction by HPLC. When the reaction was completed, dichloromethane was evaporated and diluted with water and Acetonitrile and then loaded onto a reverse phase HPLC machine (Luna C18 support, 10 u, 100A, Mobile phase A: water containing 0.1% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA, gradient began with 5% B, and changed to 50% B over 60 minutes at a flow rate of 15 ml/min). Fractions containing pure product were then freeze-dried on a lyophilyzer.

Purification

Analytical reverse-phase, high performance liquid chromatography (HPLC) was performed on a Gemini C18 column (4.6 mm×250 mm) (Phenomenex). Semi-Preparative reverse phase HPLC was performed on a Gemini 10 μm C18 column (22 mm×250 mm) (Phenomenex) or Jupiter 10 μm, 300 A ° C.18 column (21.2 mm×250 mm) (Phenomenex). Separations were achieved using linear gradients of buffer B in A (Mobile phase A: water containing 0.15% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA), at a flow rate of 1 mL/min (analytical) and 15 mL/min (preparative). Separations were achieved using linear gradients of buffer B in A (Mobile phase A: water containing 0.15% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA), at a flow rate of 1 mL/min (analytical) and 15 mL/min (preparative).

Linker Activation and Dimerization

Small Scale DIG Linker Activation Procedure:

5 mL of NMP was added to a glass vial containing IDA diacid (304.2 mg, 1 mmol), N-hydroxysuccinimide (NHS, 253.2 mg, 2.2 eq. 2.2 mmol) and a stirring bar. The mixture was stirred at room temperature to completely dissolve the solid starting materials. N, N′-Dicyclohexylcarbodiimide (DCC, 453.9 mg, 2.2 eq., 2.2 mmol) was then added to the mixture. Precipitation appeared within 10 min and the reaction mixture was further stirred at room temperature overnight. The reaction mixture was then filtered to remove the precipitated dicyclohexylurea (DCU). The activated linker was kept in a closed vial prior to use for dimerization. The nominal concentration of the activated linker was approximately 0.20 M.

For dimerization using PEG linkers, there is no pre-activation step involved. Commercially available pre-activated bi-functional PEG linkers were used.

Dimerization Procedure:

2 mL of anhydrous DMF was added to a vial containing peptide monomer (0.1 mmol). The pH of the peptide was the adjusted to 8˜9 with DIEA. Activated linker (DIG, IDA or PEG13, PEG 25) (0.48eq relative to monomer, 0.048 mmol) was then added to the monomer solution. The reaction mixture was stirred at room temperature for one hour. Completion of the dimerization reaction was monitored using analytical HPLC. The time for completion of dimerization reaction varied depending upon the linker. After completion of reaction, the peptide was precipitated in cold ether and centrifuged. The supernatant ether layer was discarded. The precipitation step was repeated twice. The crude dimer was then purified using reverse phase HPLC (Luna C18 support, 10 u, 100A, Mobile phase A: water containing 0.1% TFA, mobile phase B: Acetonitrile (ACN) containing 0.1% TFA, gradient of 15% B and changed to 45% B over 60 min, flow rate 15 ml/min). Fractions containing pure product were then freeze-dried on a lyophilyzer.

Example 2 Characterization of Peptide Dimer Molecules

The stability, potency, and selectivity of certain peptide monomer compounds and peptide dimer compounds was determined using a variety of in vitro and in vivo assays.

α4β7-MAdCAM Competition ELISA

A nickel coated plate (Pierce #15442) was coated with rh integrin α4β7 (R&D Systems #5397-A30) at 800 ng/well and incubated at room temperature with shaking for 1 hr. The solution was then removed by shaking and blocked with assay buffer (50 mM Tris-HCl pH7.6, 150 mM NaCl, 1 mM MnCl₂ or MgCl₂, 0.05% Tween-20 and 0.5% BSA) at 250 ul/well. The plate was then incubated at room temperature for 1 hr. Each well was washed 3 times with wash buffer (50 mM Tris-HCl pH7.6, 100 mM NaCl, 1 mM MnCl₂ or MgCl₂, 0.05% Tween-20). To each well was added 25 ul of a serial dilution (3-fold dilutions in assay buffer) of peptide starting at 20 μM. 25 ul of recombinant human MAdCAM-1 (R&D Systems #6056-MC) was then added to each well at a fixed concentration 20 nM. The final starting peptide concentration was 1 μM, and the final MAdCAM-1 concentration was 10 nM. The plates were then incubated at room temperature for 1 hr to reach binding equilibrium. The wells were then washed three times with wash buffer. 50 ul of mouse anti-human IgG1-HRP (Invitrogen # A10648) diluted in 1:2000 in assay buffer was then added to each well. The wells were incubated at room temperature for 45 min with shaking. The wells were then washed 3 times with wash buffer. 100 ul of 3,3′,5,5′-Tetramethylbenzidine (TMB) were then added to each well and closely observe during development time. The reaction was stopped with 2N H₂SO₄ and absorbance was read at 450 nm.

TMB is a chromogenic substrate suitable for use in ELISA procedures, which utilize horseradish peroxidase conjugates. This substrate produces a soluble end product that is blue in color and can be read spectrophotometrically at 370 or 655 nm. The reaction maybe stopped with 2 M H₂SO₄, resulting in a yellow solution that is read at 450 nm. Each tablet contains 1 mg of TMB substrate. To prepare TMB Substrate Solution, dissolve one 3,3′,5,5′-tetramethylbenzidine tablet in 1 ml of DMSO and add to 9 ml of 0.05 M Phosphate-Citrate Buffer, pH 5.0. Add 2 μl of fresh 30% hydrogen peroxide (Product No. H 1009) per 10 ml of substrate buffer solution, immediately prior to use.

α4β1-VCAM Competition ELISA

A Nunc MaxiSorp plate was coated with rh VCAM-1/CD106 Fc chimera (R&D #862-VC) at 400 ng/well in 50 ul per well in 1×PBS and incubated overnight at 4° C. The solution was removed by shaking and then blocked with 250 ul of 1% BSA in 1×PBS per well. The wells were then incubated at room temperature for 1 hr with shaking. Each well was then washed once with wash buffer (50 mM Tris-HCl pH7.6, 100 mM NaCL, 1 mM MnCl2 or MgCl₂, 0.05% Tween-20). 25 ul of serial dilutions of peptides starting at 200 μM in assay buffer (Assay buffer: 50 mM Tris-HCl pH7.6, 100 mM NaCl, 1 mM MnCl2 or MgCl₂, 0.05% Tween-20) was added to each well. Additionally, 25 ul of α4β1 (R&D Systems #5668-A4) was added to each well at a fixed concentration of 120 nM. The final peptide and α4β1 concentrations were 100 μM and 60 nM, respectively. The plates were then incubated at 37° C. for 2 hr. The solution was then removed by shaking, and each well was washed three times with wash buffer. 50 ul of 9F10 antibody at 4 ug/ml (purified mouse anti-human CD49d, BD Bioscience Cat #555502) was then added to each well, and the plate was incubated at room temperature for 1 hr with shaking. The solution was again removed by shaking, and each well was washed three times with wash buffer. 50 ul of peroxidase-conjugated AffiniPure Goat anti-mouse IgG (Jackson immune research cat #115-035-003) diluted in 1:5000 in assay buffer was added to each well. The plate was incubated at room temperature for 30 min with shaking. Each well was then washed 3 times with wash buffer. 100 ul of TMB was then added to each well and closely observe during developing time. The reaction was stepped with 2N H₂SO₄ and absorbance was read at 450 nm.

α4β7-MAdCAM Cell Adhesion Assay

RPMI 8866 human cells (Sigma #95041316) were cultured in RPMI 1640 HEPES medium (Invitrogen #22400-089) supplemented with 10% serum (Fetal Bovine Serum, Invitrogen #16140-071), 1 mM sodium pyruvate (Invitrogen #11360-070), 2 mM L-glutamine (Invitrogen #25030-081) and Penicillin-Streptomycin (Invitrogen #15140-122) at 100 units of penicillin and 100 μg of streptomycin per ml. The cells were washed two times in DMEM medium (ATCC #30-2002) supplemented with 0.1% BSA, 10 mM HEPES pH 7 and 1 mM MnCl₂. The cells were re-suspended in supplemented DMEM medium at a density of 4×10⁶ cells/ml.

A Nunc MaxiSorp plate was coated with rh MAdCAM-1/Fc Chimera (R&D #6065-MC) at 200 ng per well in 50 ul per well in 1×PBS and incubated at 4° C. overnight. The solution was then removed by shaking, blocked with 250 ul per well PBS containing 1% BSA, and incubated at 37° C. for 1 hr. The solution was removed by shaking. Peptides were diluted by serial dilution in a final volume of 50 ul per well (2× concentration). To each well, 50 ul of cells (200,000 cells) were added and the plate was incubated at 37° C., 5% CO₂ for 30-45 min to allow cell adhesion. The wells were washed manually three times (100 ul per wash) with supplemented DMEM. After the final wash, 100 ul/well of supplemented DMEM and 10 ul/well of MTT reagent (ATTC cat #30-1010K) were added. The plate was incubated at 37° C., 5% CO₂ for 2-3 hrs until a purple precipitate was visible. 100 ul of Detergent Reagent (ATTC cat #30-1010K) was added to each well. The plate was covered from the light, wrapped in Parafilm to prevent evaporation, and left overnight at room temperature in the dark. The plate was shaken for 5 min and the absorbance at 570 nm was measured. To calculate the dose response, the absorbance value of control wells not containing cells was subtracted from each test well. α4β1-VCAM Cell Adhesion Assay

Jurkat E6.1 human cells (Sigma #88042803) were cultured in RPMI 1640 HEPES medium (Invitrogen #22400-089) supplemented with 10% serum (Fetal Bovine Serum, Invitrogen #16140-071), 1 mM sodium pyruvate (Invitrogen #11360-070), 2 mM L-glutamine (Invitrogen #25030-081) and Penicillin-Streptomycin (Invitrogen #15140-122) at 100 units of penicillin and 100 μg of streptomycin per ml. The cells were washed two times in DMEM medium (ATCC #30-2002) supplemented with 0.1% BSA, 10 mM HEPES pH 7 and 1 mM MnCl₂. The cells were re-suspended in supplemented DMEM medium at a density of 4×10⁶ cells/ml.

A Nunc MaxiSorp plate was coated with rh VCAM-1/CD106 Fc chimera (R&D #862-VC) at 400 ng per well in 50 ul per well in 1×PBS and incubated at 4° C. overnight. The solution was then removed by shaking, blocked with 250 ul per well PBS containing 1% BSA, and incubated at 37° C. for 1 hr. The solution was removed by shaking. Peptides were diluted by serial dilution in a final volume of 50 ul per well (2× concentration). To each well, 50 ul of cells (200,000 cells) were added and the plate was incubated at 37° C., 5% CO₂ for 30-45 min to allow cell adhesion. The wells were washed manually three times (100 ul per wash) with supplemented DMEM. After the final wash, 100 ul/well of supplemented DMEM and 10 ul/well of MTT reagent (ATTC cat #30-1010K) were added. The plate was incubated at 37° C., 5% CO₂ for 2-3 hrs until a purple precipitate was visible. 100 ul of Detergent Reagent (ATTC cat #30-1010K) was added to each well. The plate was covered from the light, wrapped in Parafilm to prevent evaporation, and left overnight at room temperature in the dark. The plate was shaken for 5 min and the absorbance at 570 nm was measured. To calculate the dose response, the absorbance value of control wells not containing cells was subtracted from each test well.

α4β7 Cell Adhesion Assay (Mouse)

TK1 cells (ATCC # ATCC-CRL-2396) were cultured in in RPMI 1640 with 2 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate, 4.5 g/L glucose, 10 mM HEPES, and 1.0 mM sodium pyruvate (ATCC #30-2001) and supplemented with 0.1 mM non-essential amino acids, (ATCC #30-2116) 0.05 mM 2-mercaptoethanol (Invitrogen #21985) and 10% serum (Fetal Bovine Serum, Invitrogen #16140-071), and Penicillin-Streptomycin (Invitrogen #15140-122) at 100 units of penicillin and 100 μg of streptomycin per ml. The cells were washed two times in DMEM medium (ATCC #30-2002) supplemented with 0.1% BSA, 10 mM HEPES pH 7 and 1 mM MnCl₂. The cells were re-suspended in supplemented DMEM medium at a density of 4×10⁶ cells/ml.

A Nunc MaxiSorp plate was coated with Recombinant human MAdCAM-1 Fc Chimera (R&D #6065-MC) at 200 ng per well in 100 μl per well in 1×PBS and incubated at 4° C. overnight. The solution was then removed by shaking, blocked with 250 ul per well PBS containing 1% BSA, and incubated at 37° C. for 1 hr. The solution was removed by shaking. DATK 32 (anti-mouse α4β7) and peptides were diluted by serial dilution in a final volume of 50 ul per well (2× concentration). To each well, 50 ul of cells (200,000 cells) are added and the plate is incubated at 37° C., 5% CO₂ for 30-45 min to allow cell adhesion. The plate was manually washed three times with supplemented DMEM, 100 ul per wash. After the final wash, 100 ul/well of supplemented DMEM and 10 μL/well of MTT reagent (ATTC cat #30-1010K) was added to each well. Wells were incubated at 37° C. with 5% CO₂ for 2-3 hrs until purple precipitate was visible. 100 μl of Detergent Reagent (ATTC cat #30-1010K) was added to each well. The plate was then wrapped with Para film to prevent evaporation, and left overnight at room temperature in the dark. The plate was shaken for 5 min and the absorbance at 570 nm was measured. To calculate the dose response, the absorbance value of control wells not containing cells was subtracted from each test well.

PBMC Memory T Cell Adhesion Assay

Fresh CD4+/CD45RO+ memory T cells were isolated from human peripheral blood mononuclear cell (PBMC) donors by Aragen Bioscience Inc. (Morgan Hill, Calif.). The assay plate was prepared using IgG Fc capture antibody (donkey anti human) immobilized at 500 ng/well in 50 mM sodium bicarbonate buffer, pH 9.5, ON, 4 C onto a Greiner Fluotrac plate (100 ul per well). The plate was rinsed two time with Blocking Buffer (25 mM Tris HCl, pH7.5, 150 mM NaCl, 1.5% BSA, 0.05% Tween), and blocked with Blocking Buffer for 2 hours at 37 C or 5 hours at RT using 200 ul per well. The Blocking Buffer was removed and either MAdCAM-1 or VCAM-1 at 400 ng/well in Blocking Buffer was added and the plate incubated overnight at 4 C (100 ul per well). The plate was washed two times with Blocking Buffer, and rinsed once with 200 ul Binding Media (DMEM phenol red free, 10 mM HEPES, 1×Na pyruvate, 1× Glutamine, and supplemented with 1 mM MnCl2 prior to use). To prepare cells, approximately 25 million CD4+/CD45RO+ memory T cells were counted by trypan blue exclusion using a haemocytometer to determine viability and cell count. The cells were transferred to a 50 ml conical tube, and centrifuged at 1200 rpm for 10 minute. The media was aspirated and the cell pellet resuspended in 15 ml Binding Media. The cells were centrifuged again and resuspended in the appropriate amount of Binding Media to be used for assays (50 ul of cells per well at 2× the final density). To each well, and equal volume (50 ul) of test compound was added and the plate was incubated for 1.5 hours at 37 C, 5% CO₂. Each well was rinsed 3× with 150 ul per well of Binding Media. CyQuant NF reagent was prepared as suggested by manufacturer), and 100 ul of CyQuant NF reagent was added per well. The plate was incubated at 37 C, 5% CO₂, for 45 minutes. The plate was protected from light by using black adhesive seals. Fluorescence intensity was measured using a Molecular Devices Gemini EM Fluorescent Plate Reader (Ex 485/Em530, Bottom Read, Reading Sensitivity=20). IC50 curves are generated using Graph Pad Prism and the curves analyzed using analyzed using a non-linear regression (four parameters) algorithm. The log (concentration) versus RFU (Ex485/Em530) was plotted to determine IC50 values.

Simulated Intestinal Fluid (SIF) Stability Assay

Studies were carried out in simulated intestinal fluid (SIF) to evaluate intestinal stability of the peptide molecules of the instant invention. To prepare the SIF reagent, blank FASSIF was prepared by dissolving 0.348 g NaOH, 3.954 g sodium phosphate monobasic monohydrate and 6.186 g NaCl in a final volume of 1 liter water (final pH=6.5). To this solution, 24 g porcine pancreatin (Sigma catalog P7545) was added and stirred for 30 minutes (final pancreatin concentration is 2.4%). The solution was filtered through a cheese cloth and a No. 1 Whatman filter, and 10 ml aliquots were stored at −70° C. To run the reaction, a 10 ml aliquot was thawed at 37° C., and 125 μl aliquots were removed and mixed with an equal volume of blank FASSIF. The peptide stock solution (10 mM in 100% DMSO) was diluted 75-fold in blank FASSIF. A 50 μl aliquot of the diluted peptide was combined with 125 μl pancreatin (2.4%) and 125 μl blank FASSIF to yield final concentrations of 1% pancreatin and 2 μM peptide. The reactions were incubated at 37° C., and at various time points 50 μl aliquots were removed and added to 200 μl of quench solution containing 50% acetonitrile, 50% methanol, 5% formic acid, and 1 μg/ml internal standard. The quenched samples were centrifuged at 10,000 rpm for 10 minutes, and the supematants were analyzed by LCMS/MS. The percent remaining at each time point was calculated based on the peak area response ratio of test to compound to internal standard. Half-lives were calculated by fitting to a first-order exponential decay equation using GraphPad.

Intestinal Wash Assay

Intestinal wash assay solution was prepared from rats fasted for at least 6 hours prior. The animals were euthanized and a midline incision was made from the point of the jaw to the pubis. The abdomen and chest were opened by making 2 incisions through the anterior chest wall on either side. Hemostats were used to clamp off both ends of the animal's stomach—where the esophagus meets the stomach and where the stomach meets the duodenum. A hemostat was also used to clamp 2-3 cm down the intestine from where the stomach meets the duodenum.

Intestinal wash assay solution was prepared by separating 20 cm of the small intestine from the body. Once separated 20 cm, the end was clamped with a hemostat and the section cut from the body, leaving the hemostats in place on the removed section. 1 mL of chilled saline was drawn up with a 1 mL syringe. One end of the intestine was held up and the clamp removed. Approximately 2-2.5 cm of the gavage needle was inserted into the intestine, and the saline was slowly injected. The fluid was massaged down the length of the intestine using gloved fingers. The gavage needle was removed and the clamp was replaced on the end of the intestine. The intestine was sat straight and a q-tip was run firmly up and down the length of the outside of the intestine approximately 3-6 times to mix the enzymes with the saline. One end of the intestine was held up and some of the fluid was carefully moved at the top down. The clamp was removed and that end of the intestine was set into a small weigh boat on ice. The other end of the intestine was carefully picked up and held vertically. Gloved fingers were gently run down it to squeeze the fluid into the container. The previous steps saline injection and fluid procurement steps were repeated twice using only 0.5 mL of chilled saline. The sample was pipetted from the weigh boat into a centrifuge tube and placed on ice. All intestinal wash samples were spun down in a cold centrifuge at 12,000×g for 10 minutes. The supernatant from the top of each centrifuged sample was pipetted into cryotubes, and kept on ice until use.

Intestinal wash assays were performed using intestinal wash assay solution prepared as described above. A sufficient amount of rat intestinal wash was thawed. For each sample, 200 uL of rat intestinal wash fluid was pipetted into 1.5 mL Eppendorf tubes (number of tubes for experiment=number of test peptides×N). The tubes were pre-incubated for about 10 minutes in a water bath at 37° C.

Peptide working solutions (2 mM) were prepared by combining 2 μl of 10 mM DMSO stock with 128 μl 100 mM Tris pH 7.5.

Peptide quench solvent (50% ACN-50% MeOH-5% Formic Acid)+IS (5 ug/ml; 1 ul of 10 mg/mL IS per 2 mL quench solvent) was prepare and a quench plate prepared and placed on ice. 200 ul of quench solution was added to each well of the quench plate for T=0, 10, 20, 30, 60 and 180 min collection.

For each test sample and a positive control, 30 ul of peptide working solution was added to a tube of intestinal wash fluid. The tube was gently vortexed and 30 ul was immediately removed and quenched in T=0 well of quench plate (pipetted directly into the quench solution). This well was covered tightly to prevent evaporation. 30 ul aliquots were removed at T=10 min, T=20 min, T=30 min, T=60 min, and T=180 min, and quenched. When all time points were collected, the quench plate was centrifuged at 10,000 rpm for 10 minutes. 150 uL of each supernatant was transferred to a polypropylene 96-well collection plate. 300 ul Mobile Phase A was added to each collection, and LC/MS/MS analysis was performed to determine the amount or concentration of peptide remaining in each test sample and positive control.

Simulated Gastric Fluid (SGF) Assay

SGF was prepared by adding 20 mg NaCl, 32 mg porcine pepsin (MP Biochemicals, catalog 02102599), and 70 μl HCl to 10 ml water (final pH=2). Aliquots of SGF (0.5 ml each) were pre-warmed at 37° C. For each peptide tested, to start the reaction, 1 μl of peptide stock solution (10 mM in DMSO) was added to 0.5 ml SGF and thoroughly mixed such that the final peptide concentration was 20 μM. The reactions were incubated at 37° C. with gentle shaking. At each time point (0, 15, 30, 60 min), 50 μl aliquots were removed and added to 200 ul acetonitrile containing 0.1% formic acid to quench the reaction. Samples were stored at 4° C. until the end of the experiment and centrifuged at 10,000 rpm for 5 minutes. Aliquots of the supernatant were removed, diluted 1:1 into distilled water containing internal standard, and analyzed by LCMS/MS. Percent remaining at each timepoint was calculated based on the peak area response ratio of test compound to internal standard. Time 0 was set to 100%, and all later timepoints were calculated relative to time 0. Half-lives were calculated by fitting to a first-order exponential decay equation using GraphPad.

Plasma Stability Assay

0.5 mL of rat plasma (one tube per peptide, volume depends on how many time points are to be collected, 50 μL per time point) was added to each well of a 96-well polypropylene plate, and the tubes were incubated in a heated water bath, preset to 37° C. with gentle shaking. 1 μL of 10 mM peptide stock solution was added to each tub, and then 200 L of Acetonitrile w/0.1% Formic Acid was added to each tube (1:4). Samples were collected at the following time points: 0, 10, 30, 45, 60, 120, 180 mins. When all time points were collected, the plate was centrifuged at 5000 rpm for 5 mins. LCM analysis was performed by pipetting 100 μL of each sample to appropriate well of a 96-well deep plate. 100 μL of an internal standard peptide (1 μg/mL) was added in Mobile Phase A to each well. The plate was vortexed and injected

Dithiothreitol (DTT) Redox Stability Assay

For each peptide tested, the DTT stability assay was conducted by adding 5 μl of a 10 mM peptide stock solution in DMSO to 1 ml of 100 mM Tris-Cl, pH 7.5 (final peptide concentration is 50 μM). At time 0 min, 5 ul of a freshly thawed 100 mM DTT solution was added to the incubation tube containing the peptide, such that the final DTT concentration was 0.5 mM. The reactions were incubated at room temperature. At different time points up to 120 minutes (20 min, 40 min, 80 min, 120 min), 50 μl aliquots were removed, and the reaction was quenched by adding 10 μl of 5M acetic acid. To measure disappearance of the parent peptide, the quenched samples (30 μl) were analyzed by reverse phase HPLC and UV absorbance at 220 nm. The fraction oxidized remaining was graphed versus time, and half-lives were calculated by fitting to a first-order exponential decay equation using Excel.

Cysteine/Cystine Redox Stability Assay

Peptides were diluted to 90 μM by adding 4.545 μl of a 10 mM peptide DMSO stock to 495.45 μl of 100 mM Tris-Cl, pH 7.5. Aliquots of 75 μl were transferred to 8 wells down a column of a 96 well plate. 20 μl of 2.5 mM Cystine in 100 mM Tris-Cl, pH 7.5 was added to each well. Cysteine stock solutions in 100 mM Tris-Cl, pH 7.5 were prepared fresh at the following concentrations: 400 mM, 200 mM, 80 mM, 44 mM, 22 mM, 11 mM, 5.5 mM and blank. At time 0, 25 μl of each cysteine stock solution was added to the 55 μl of cystine/peptide solution, and the mixture was incubated at room temperature for 40 min. The samples were quenched by adding 20 μl of 5M acetic acid and analyzed by reverse phase HPLC. The fraction of oxidized peptide was calculated and plotted against the calculated oxidation reduction potential (ORP) as defined by the Nernst equation. The ORP where half of the oxidized peptide remains is shown below.

[Cysteine], mM [Cystine], mM ORP, mV 1.375 0.5 −176 2.375 0.5 −194 5.5 0.5 −213 11 0.5 −231 20 0.5 −247 50 0.5 −271 100 0.5 −290

Table 3 provides data demonstrating the potency, selectivity and stability of various peptide monomers and dimers of the present invention. The amino acid sequences of peptide monomers or peptide dimer subunits are provided in Table 3A, shown from N-terminus to C-terminus from left to right, and identified by a sequence identifier number. The accompanying data for each peptide is shown in Tables 3B and 3C. Dimers are indicated by parentheses followed by a subscripted 2. N-terminal and C-terminal groups are indicated, e.g., Ac and NH₂, respectively. Dimers are linked at the C-termini of their monomer subunits, and the linker is indicated to the right of the peptide sequence. Each of the peptide sequences shown includes a disulfide linkage between the amino acid residues located at position 4 and position 10, e.g., Pen and Pen. Table 4 provides comparative data demonstrating the greater potency, selectivity and stability of peptide monomer compounds and peptide dimer compounds of the present invention. The amino acid sequences of peptide monomers or peptide dimer subunits are provided in Table 4A, shown from N-terminus to C-terminus from left to right, and identified by a sequence identifier number. The accompanying data for each peptide is shown in Tables 4B and 4C. Dimers are indicated by parentheses followed by a subscripted 2. N-terminal and C-terminal groups are indicated, e.g., Ac and NH₂, respectively. Each of the peptide sequences shown includes a disulfide linkage between the amino acid residues located at position 4 and position 10, e.g., Pen and Pen. For the stability assay data, assays were conducted for varying durations of time, so an indication that t_(1/2) was greater than a certain value means that the assay was stopped at that time, before half life could be determined. For DTT assays, where data is not shown for peptides comprising two Pen residues, the predicted DTT assay stability is greater than two hours.

TABLE 3-A Sequence and Structure of Illustrative Peptide Monomers and Peptide Dimers SEQ ID NO: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 1 (Ac Pen N—Me—R S D T L Pen W Beta-E k NH2)2 DIG 2 (Ac Pen N—Me—R S D T L Pen f e k NH2)2 DIG 3 (Ac Pen N—Me—R S D T L Pen F(4-CF3) e k NH2)2 DIG 4 (Ac k C N—Me—R S D T L C W k NH2)2 DIG 5 DIG (Ac k C N—Me—R S D T L C W k NH2)2 DIG 6 DIG NH2 C N—Me—R S D T L C W NH2 7 DIG NH2 Pen N—Me—R S D T L Pen f NH2 8 Ac Pen N—Me—R S D T L Pen 1-NaI e k NH2 9 Ac Pen N—Me—R S D T L Pen 2-NaI e k NH2 10 Ac Pen N—Me—R S D T L Pen D-1-NaI E k NH2 11 Ac Pen N—Me—R S D T L Pen D-2-NaI E k NH2 12 Ac Pen N—Me—R S D T L Pen 1-NaI e N—Me-k NH2 13 Ac Pen N—Me—R S D T L Pen 2-NaI e N—Me-k NH2 14 Ac Pen N—Me—R S D T L Pen HPhe e k NH2 15 Ac Pen N—Me—R S D T L Pen 2-NaI E N—Me-k NH2 16 Ac Pen N—Me—R S D T L Pen F(2,4-diCl) E k NH2 17 Ac Pen N—Me—R S D T L Pen F(3,4-diCl) E k NH2 18 Ac Pen N—Me—R S D T L Pen 1-NaI E N—Me-k NH2 19 Ac Pen N—Me—R S D T L Pen HPhe E k NH2 20 PEG13 NH2 C N—Me—R S D T L Pen W NH2 21 PEG25 NH2 C N—Me—R S D T L Pen W NH2 22 (Ac Pen N—Me—R S D T L Pen Y E k NH2)2 DIG 23 (Ac Pen N—Me—R S D T L Pen 2-NaI Y k NH2)2 DIG 24 (Ac Pen N—Me—R S D T L Pen 1-NaI E k NH2)2 DIG 25 (Ac Pen N—Me—R S D T L Pen H E k NH2)2 DIG 26 (Ac Pen N—Me—R S D T L Pen H Y k NH2)2 DIG 27 (Ac Pen N—Me—R S D T L Pen 2-NaI y k NH2)2 DIG 28 (Ac Pen N—Me—R S D T L Pen w E k NH2)2 DIG 29 (Ac Pen N—Me—R S D T L Pen 2-NaI e k NH2)2 DIG 30 (Ac Pen N—Me—R S D T L Pen f E k NH2)2 DIG 31 (Ac Pen N—Me—R S D T L Pen W N—Me-E k NH2)2 DIG 32 (Ac Pen N—Me—R S D T L Pen 1-NaI e k NH2)2 DIG 33 (Ac Pen N—Me—R S D T L Pen 2-NaI e k NH2)2 DIG 34 (Ac Pen N—Me—R S D T L Pen D-1-NaI E k NH2)2 DIG 35 (Ac Pen N—Me—R S D T L Pen D-2-NaI E k NH2)2 DIG 36 (Ac C N—Me—R S D T L Pen W k NH2)2 PEG13 37 (Ac C N—Me—R S D T L Pen W k NH2)2 PEG25 38 (Ac Pen N—Me—R S D T L Pen 1-NaI e N—Me-k NH2)2 DIG 39 (Ac Pen N—Me—R S D T L Pen 2-NaI e N—Me-k NH2)2 DIG 40 (Ac Pen N—Me—R S D T L Pen HPhe e k NH2)2 DIG 41 (Ac Pen N—Me—R S D T L Pen 2-NaI E N—Me-k NH2)2 DIG 42 (Ac Pen N—Me—R S D T L Pen F(2,4-diCl) E k NH2)2 DIG 43 (Ac Pen N—Me—R S D T L Pen F(3,4-diCl) E k NH2)2 DIG 44 (Ac Pen N—Me—R S D T L Pen 1-NaI E N—Me-k NH2)2 DIG 45 (Ac Pen N—Me—R S D T L Pen HPhe E k NH2)2 DIG 46 Ac Pen N—Me—R S D D L Pen W E k NH2 47 Ac Pen N—Me—R S Prop T L Pen W E k NH2 acid 48 Ac Pen N—Me—R d D T L Pen W E k NH2 49 Ac Pen N—Me—R S D T L Pen W E P k NH2 50 Ac Pen N—Me—R S D T L Pen 2-NaI Hphe k NH2 51 Ac Pen N—Me—R S D T L Pen W Aic k NH2 52 NH2 Beta-Ala Pen N—Me—R S D T L Pen W E NH2 53 NH2 Beta-Ala Pen N—Me—R S D T L Pen W e NH2 54 DIG (NH2 Beta-Ala Pen N—Me—R S D T L Pen W E NH2)2 55 Ac Pen N—Me—R S D T L Pen W e Dap NH2 56 Ac Pen N—Me—R S D T L Pen W e Dab NH2 57 Ac Pen N—Me—R S D T L Pen W E NH2 58 Ac Pen N—Me—R S D T L Pen W e NH2 59 Ac Pen N—Me—R S D T L Pen W E Dap NH2 60 Ac Pen N—Me—R S D T L Pen W E Dap Ac 61 Ac Pen N—Me—R S D T L Pen W E Dab NH2 62 Ac Pen N—Me—R S D T L Pen W E Dab Ac 63 Ac Pen N—Me—R S D T L Pen W e Dap Ac 64 Ac Pen N—Me—R S D T L Pen W e Dab Ac 65 Ac Pen N—Me—R S D T L Pen W E k Ac 66 Ac Pen N—Me—R S D T L Pen W e k Ac 67 (Ac Pen N—Me—R S D T L Pen W E k NH2)2 DIG 68 (Ac Pen N—Me—R S D T L Pen W e k NH2)2 DIG 69 Ac Pen N—Me—R S D(OMe) T L Pen W E k NH2 Biotine 70 (Ac Pen N—Me—R S D T L Pen W e k NH2)2 IDA 71 (Ac Pen N—Me—R S D T L Pen W e k NH2)2 IDA Biotine 72 (Ac Pen N—Me—R S D T L Pen W e k NH2)2 IDA PEG4 Biotine 73 (Ac Pen N—Me—R S D(OMe) T L Pen W E k NH2)2 DIG 74 Ac D-Pen N—Me—R S D T L Pen W e k NH2 75 Ac Pen N—Me—R S D T L Pen 2-NaI E NH2 76 (Ac Pen N—Me—R S D T L Pen W k OH)2 DIG 77 (Ac Pen N—Me—R S D T L Pen W N—Me—K NH2)2 DIG 78 (Ac Pen N—Me—R S D T L Pen W E k OH)2 DIG 79 (Ac Pen N—Me—R S D T L Pen 2-NaI Bip k NH2)2 DIG 80 (Ac Pen N—Me—R S D T L Pen Tic e k NH2)2 DIG 81 (Ac Pen N—Me—R S D T L Pen W E k NH2)2 IDA PEG4 Biotine 82 (Ac Pen N—Me—R S D T L Pen W Q k NH2)2 DIG 83 (Ac Pen N—Me—R S D T L Pen W N k NH2)2 DIG 84 (Ac Pen N—Me—R S D T L Pen W Cit k NH2)2 DIG 85 (Ac Pen N—Me—R S D T L Pen W F k NH2)2 DIG 86 (Ac Pen N—Me—R S D T L Pen W E(OMe) k NH2)2 DIG 87 (Ac Pen N—Me—R S D T L Pen W D k NH2)2 DIG 88 Ac Pen N—Me—R S D T L Pen 2-NaI k NH2 89 Ac Pen N—Me—R S D T L C Tic e k NH2 90 Ac Pen N—Me—R S D T L Pen 2-NaI k NH2 DIG 91 (Ac Pen N—Me—R S D T L Pen W f k NH2)2 DIG 92 (Ac Pen N—Me—R S D T L Pen W y k NH2)2 DIG 93 (Ac Pen N—Me—R S D T L C Tic e k NH2)2 DIG 94 (Ac Pen N—Me—R S D T L Pen W P k NH2)2 DIG 95 (Ac Pen N—Me—R S D T L Pen W P K NH2)2 DIG 96 (Ac Pen N—Me—R S D T L Pen W P K NH2)2 DIG 97 (Ac Pen N—Me—R S D T L Pen W E Dab NH2)2 DIG 98 (Ac Pen N—Me—R S D T L Pen F(2-carbamoyl) e k NH2)2 DIG 99 (Ac Pen N—Me—R S D T L Pen F(3-carbamoyl) e k NH2)2 DIG 100 (Ac Pen N—Me—R S D T L Pen F(4-COOH) e k NH2)2 DIG 101 (Ac Pen N—Me—R S D T L Pen F(2,4-ci) e k NH2)2 DIG 102 (Ac Pen N—Me—R S D T L Pen F(3,4-ci) e k NH2)2 DIG 103 (Ac Pen N—Me—R S D T L Pen F(4-OMe) e k NH2)2 DIG 104 (Ac Pen N—Me—R S D T L Pen W h k NH2)2 DIG 105 (Ac Pen N—Me—R S D T L Pen W F(4-COOH) k NH2)2 DIG 106 (Ac Pen N—Me—R S D T L Pen F(4tBu) e k NH2)2 DIG 107 (Ac Pen N—Me—R S D T L Pen F(4-F) e k NH2)2 DIG 108 (Ac Pen N—Me—R S D T L Pen Bip e k NH2)2 DIG 109 (Ac Pen N—Me—R S D T L Pen W Tic k NH2)2 DIG 110 (Ac Pen N—Me—R S D T L Pen W w k NH2)2 DIG 111 (Ac Pen N—Me—R S D T L Pen 1-NaI f k NH2)2 DIG 112 (Ac Pen N—Me—R S D T L Pen 1-NaI h k NH2)2 DIG 113 (Ac Pen N—Me—R S D T L Pen 1-NaI 1 k NH2)2 DIG 114 (Ac Pen N—Me—R S D T L Pen 1-NaI r k NH2)2 DIG 115 (Ac Pen N—Me—R S D T L Pen 1-NaI Tic k NH2)2 DIG 116 (Ac Pen N—Me—R S D T L Pen 1-NaI t k NH2)2 DIG 117 (Ac Pen N—Me—R S D T L Pen 2-NaI f k NH2)2 DIG 118 (Ac Pen N—Me—R S D T L Pen 2-NaI h k NH2)2 DIG 119 (Ac Pen N—Me—R S D T L Pen 2-NaI 1 k NH2)2 DIG 120 (Ac Pen N—Me—R S D T L Pen 2-NaI r k NH2)2 DIG 121 (Ac Pen N—Me—R S D T L Pen 2-NaI Tic k NH2)2 DIG 122 (Ac Pen N—Me—R S D T L Pen F(4CF3) e k NH2)2 DIG 123 (Ac Pen N—Me—R S D T L Pen Y e k NH2)2 DIG 124 (Ac Pen N—Me—R S D T L Pen H e k NH2)2 DIG 125 (Ac Pen N—Me—R S D T L Pen F(4tBu) E k NH2)2 DIG 126 (Ac Pen N—Me—R S D T L Pen F(4tBu) E N—Me—K NH2)2 DIG 127 Ac Pen N—Me—R S D T L Pen W OH 128 Ac Pen N—Me—R S D T L Pen W E OH 129 (Ac Pen N—Me—R S D T L Pen F(4-COOH) E k NH2)2 DIG 130 (Ac Pen N—Me—R S D T L Pen F(4-COOH) b-H-E k NH2)2 DIG 131 (Ac Pen N—Me—R S D T L Pen F(4tBu) E k NH2)2 DIG 132 (Ac Pen N—Me—R S D T L Pen F(4tBu) b-H-E k NH2)2 DIG 132 (Ac Pen N—Me—R S D T L Pen F(4tBu) b-H-E k NH2)2 DIG Acetate salt 133 (Ac Pen N—Me—R S D T L Pen F(4tBu) E N—Me—K NH2)2 DIG 134 (Ac Pen N—Me—R S D T L Pen Bip E k NH2)2 DIG 135 (Ac Pen N—Me—R S D T L Pen Bip b-H-E k NH2)2 DIG 136 (Ac Pen N—Me—R S D T L Pen Bip E N—Me—K NH2)2 DIG 137 (Ac Pen N—Me—R S D T L Pen 2-NaI b-H-E k NH2)2 DIG 138 (Ac Pen N—Me—R S D T L Pen 2-NaI E N—Me—K NH2)2 DIG 139 (Ac Pen N—Me—R S D T L Pen F(4-CN) b-H-E k NH2)2 DIG 140 (Ac Pen N—Me—R S D T L Pen 2-NaI t k NH2)2 DIG 141 (Ac Pen N—Me—R S D T L Pen W b-H-E N—Me—K NH2)2 DIG 142 (Ac Pen N—Me—R S D T L Pen 1-NaI b-H-E N—Me—K NH2)2 DIG 143 Cyclo [Pen N—Me—R S D T L Pen 2-NaI E] 144 Cyclo [Pen N—Me—R S D T L Pen W E] 145 Cyclo [Pen N—Me—R S D T L Pen W e] 146 Ac Pen N—Me—R S D T L Pen W b-H-E OH 147 (Ac Pen N—Me—R S D T L Pen F(4-COOH) E N—Me—K NH2)2 DIG 148 (Ac Pen N—Me—R S D T L Pen F(4-COOH) b-H-E N—Me—K NH2)2 DIG 149 (Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E N—Me—K NH2)2 DIG 150 (Ac Pen N—Me—R S D T L Pen Bip b-H-E N—Me—K NH2)2 DIG 151 Ac Pen N—Me—R S D T L Pen F(4-tBu) OH 152 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E OH 153 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2 154 Ac Pen N—Me—R S D T L Pen Tic b-H-E NH2 155 Ac Pen N—Me—R S D T L Pen 2-NaI b-H-E NH2 156 Ac Pen N—Me—R S D V L Pen 2-NaI e NH2 157 Ac Pen N—Me—R S D F L Pen 2-NaI e NH2 158 Ac Pen N—Me—R S D Cha L Pen 2-NaI e NH2 159 Ac Pen N—Me—R S D L L Pen 2-NaI e NH2 160 Ac Pen N—Me—R S D I L Pen 2-NaI e NH2 161 Ac Pen N—Me—R S D hLeu L Pen 2-NaI e NH2 162 Ac Pen N—Me—R S D T F Pen 2-NaI e NH2 163 Ac Pen N—Me—R S D T Q Pen 2-NaI e NH2 164 Ac Pen N—Me—R S D T Y Pen 2-NaI e NH2 165 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E NH2 166 (Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2)2 IDA 167 (Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2)2 IDA PEG4 Biotin 168 (Ac Pen N—Me—R S D T L Pen F(4tBu) b-H-E k OH)2 DIG 169 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k 4,4,4Triflouro butyric acid 170 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k Hexanoic acid 171 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k Isovalaric acid 172 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k Palmitoyl chloride 173 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k Lauroyl chloride 174 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k Oleoyi chloride 175 Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k Myristoy chloride 176 Hexanoic Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2 acid 177 Isovalaric Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2 acid 178 Palmitoyl Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2 chloride 179 Lauroyl Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2 chloride 180 Oleoyi Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2 chloride 181 Myrstoy Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2 chloride 182 (Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2)2 IDA Alexa-488 182 (Ac Pen N—Me—R S D T L Pen F(4-Bu) b-H-E k NH2)2 IDA Alexa-488 183 (Ac Pen N—Me—R S D T L Pen F(4-Bu) b-H-E k NH2)2 IDA Alexa-647 184 (13C(2)-Ac Pen N—Me—R S D T L Pen F(4tBu) b-H-E k NH2)2 DIG 185 (Ac Pen N—Me—R S D T 13C(5)L Pen F(4tBu) b-H-E k NH2)2 DIG 186 (Ac Pen N—Me—R S D I L Pen F(4-tBu) b-H-E k NH2)2 IDA 187 (Ac Pen N—Me—R S D T Q Pen F(4-tBu) b-H-E k NH2)2 IDA 188 (Ac Pen N—Me—R S D I L Pen F(4-tBu) b-H-E k NH2)2 IDA Alexa-647 189 (Ac Pen N—Me—R S Q I Q Pen F(4-tBu) b-H-E k NH2)2 DIG 190 (Ac Pen N—Me—R S Q I Q Pen F(4-tBu) b-H-E k NH2)2 IDA 191 (Ac Pen N—Me—R S D D L Pen F(4-tBu) b-H-E k NH2)2 IDA 192 (Ac Pen N—Me—R S Q I Q Pen F(4-tBu) b-H-E k NH2)2 IDA Alexa-647 193 (Ac Pen N—Me—R S D D L Pen F(4-tBu) b-H-E k NH2)2 IDA Alexa-647

TABLE 3-B Potency, Selectivity, and Stability of Illustrative Peptide Monomers and Dimers Potency (α4β7) Selectivity (α4β1) α4β7 α4β7 cell α4β7 cell α4β1 α4β1 cell PBMC Stability SEQ ELISA IC50 (Hu) IC50 (Mu) IC50 ELISA IC50 IC50 IC50 SIF t½ ID NO: (nM) (nM) (nM) (nM) (nM) (nM) (min) 1 >50 >180 2 >100 >180 3 >25 >180 4 >10 <20 5 >50 6 6 >50 7 >1,000 8 >25 9 >10 >100 10 >10 11 >25 12 >25 13 >10 >100 14 >25 15 ≤10 16 >10 17 >10 18 >10 >500 19 >10 20 >50 21 >50 22 ≤10 ≤10 >100 <20 23 ≤10 >100 <20 24 ≤10 ≤10 >100 56 25 >10 26 >100 27 >25 >180 28 >50 29 ≤10 >10 >180 30 >100 31 >50 32 ≤10 >10 >100 >180 33 ≤10 >10 >100 >100,000 >180 34 >25 35 >100 36 >50 37 >100 38 ≤10 ≤10 >100 >180 39 >10 >180 40 ≤10 >100 41 ≤10 ≤10 >100 >180 42 ≤10 ≤10 >100 51, 49 43 ≤10 >10 >100 21 44 ≤10 ≤10 ≤10 >100 >180 45 >25 37 46 >1,000 >180 47 >1,000 >180 48 >1,000 >180 49 >10 >180 50 >10 104 51 >25 180 52 >10 >100 117 53 >10 >180 54 >25 >100 32 55 >100 >180 56 >500 >180 57 58 59 >10,000 60 >1,000 61 >1,000 62 >1,000 63 >1,000 64 >1,000 65 >10,000 66 >10,000 67 ≤10 ≤10 ≤10 >100 >100,000 121 68 ≤10 >25 ≤10 >500 >100,000 >100 >300 69 >10 >100 70 >25 71 >25 72 >25 73 ≤10 ≤10 74 75 >50 76 >10 77 >100 >180 78 ≤10 ≤10 ≤10 >100 >100,000 79 80 >50 >180 81 82 >50 83 >50 84 >10 <20 85 ≤10 86 ≤10 ≤10 87 >25 88 >10 89 >25 90 91 >100 92 >50 93 >500 94 >100 95 >100 96 >50 97 ≤10 98 >50 99 >100 >180 100 ≤10 101 >50 102 >100 103 >25 104 >100 35 105 >50 106 ≤10 107 >25 >180 108 >10 109 >100 110 >10 111 >100 112 >50 113 >500 114 >100 115 >100 116 >50 117 >100 118 >25 119 >500 120 >1,000 121 >100 122 >50 123 >50 124 >100 125 >100 126 >1,000 127 >100 35 hr 128 >50 180 129 ≤10 ≤10 >100 ≤10 >360 (13 hr) 130 ≤10 ≤10 >100 ≤10 >360 (16 hr) 131 ≤10 ≤10 >100 >360 (9 hr) 132 ≤10 ≤10 ≤10 >100 >100,000 ≤10 >360 (10.7 h) 132 ≤10 ≤10 ≤10 >500 ≤10 11 hr 133 ≤10 ≤10 >100 ≤10 >360 (11 hr) 134 ≤10 ≤10 >100 135 ≤10 136 ≤10 137 ≤10 ≤10 >1,000 138 >10 >10 139 ≤10 140 >10 141 ≤10 ≤10 >500 142 ≤10 ≤10 >500 >50 143 250 >10,000 144 364 >10,000 145 504 >10,000 146 >50 >50 >1,000 147 ≤10 ≤10 ≤10 >100 ≤10 >300 148 ≤10 ≤10 ≤10 >100 >300 149 ≤10 ≤10 ≤10 >500 ≤10 >300 150 ≤10 ≤10 ≤10 >1,000 >300 151 >10 >50 187 152 ≤10 ≤10 ≤10 >100 >25 147 153 >10 >10 >10 >1,000 13.6 hr   154 >100 >1,000 >1,000 155 >25 >25 >1,000 156 >100 157 >1,000 158 >1,000 159 >1,000 160 >1,000 161 >1,000 162 >1,000 163 >1,000 164 >1,000 165 >10 >100 >180 166 ≤10 ≤10 167 ≤10 ≤10 168 ≤10 ≤10 169 >10 170 >10 171 >10 172 965 173 >100 174 >1,000 175 >500 176 >50 177 >50 178 >1,000 179 >100 180 >1,000 181 >1,000 182 ≤10 >180 182 ≤10 0 >180 183 ≤10 0 >180 (466) 184 185 186 >100 187 >100 188 ≤10 189 >10,000 190 >100,000 191 >10,000 192 >10,000 193 >100,000 For IC50 data: ≤10 is less than or equal to 10 nM; >10 is greater than 10 nM and less than or equal to 25 nM; >25 is greater then 25 nM and less than or equal to 50 nM; >50 is greater than 50 nM and less than or equal to 100 nM; >100 is greater than 100 nM and less than or equal to 500 nM; >500 is greater than 500 nM and less than or equal to 1,000 nM; >1,000 is greater than 1,000 nM and less than or equal to 10,000 nM; >10,000 is greater than >10,000 nM but less than or equal to >100,000 nM; and >100,000 is greater than 100,000 nM. For stability data: >180 means experiment was stopped after 180 min and half life was not reached; >360 means experiment was stopped after 360 min and half life was not reached.

TABLE 4-A Comparison of Peptide Monomers and Dimers - Sequences peptide 1 2 3 4 5 6 7 8 9 10 11 12 13 14 194 Ac C R S D T L C G E NH2 195 Ac C R S D T L C NH2 196 Ac C R S D T L C G E K NH2 197 (Ac C R S D T L C G E K NH2)2 PEG25 198 Ac C N—Me—R S D T L C G E NH2 199 Ac C N—Me—R S D T L C G E K OH 200 (Ac C N—Me—R S D T L C K OH)2 PEG25 201 (Ac C N—Me—R S D T L C G E K OH)2 DIG 202 Ac C N—Me—R S D T L Pen k NH2 203 (Ac C N—Me—R S D T L Pen k NH2)2 IDA 204 (Ac C N—Me—R S D T L Pen W k NH2)2 DIG 205 (Ac C N—Me—R S D T L Pen E k NH2)2 DIG 206 Ac Pen R S D T L C k NH2 207 (Ac Pen R S D T L C k NH2)2 DIG 208 Ac Pen N—Me—R S D T L Pen W k NH2 209 (Ac Pen N—Me—R S D T L Pen W k NH2)2 DIG 210 Ac Pen N—Me—R S D T L Pen 2-NaI E k NH2 211 (Ac Pen N—Me—R S D T L Pen W e k NH2)2 DIG 212 (Ac Pen N—Me—R S D T L Pen 2-NaI E k NH2)2 DIG 213 (Ac Pen N—Me—R S D T L Pen W b-h-E k NH2)2 DIG 214 (Ac Pen N—Me—R S D T L Pen W E N—Me-k NH2)2 DIG 215 (Ac Pen N—Me—R S D T L Pen W E N—Me—K NH2)2 DIG 216 (Ac Pen N—Me—R S D T L Pen W e k OH)2 DIG 217 (Ac Pen N—Me—R S D T L Pen W E k NH2)2 DIG 218 (Ac Pen N—Me—R S D T L Pen F(4-tBu) b-H-E k NH2)2 DIG

TABLE 4-B Comparison of Peptide Monomers and Dimers - Potency and Selectivity Cell Cell Cell Adhesion Cell ELISA Adhesion Adhesion α4β7 Adhesion α4β7 ELISA_α4β1 α4β7 α4β1 Mouse PBMC IC50 peptide IC50 (nM) IC50 (nM) IC50 (nM) IC50 (nM) IC50 (nM) (nM) 194 97 2020 590 195 97 2880 1221 196 87 4810 6660 >100,000 197 36 964 301 >100,000 198 20 1287 1120 >100,000 199 58 >100,000 4691 200 3 16667 96 >100,000 201 1 1244 28 202 87 1619 11049 >100,000 203 7.5 700 200 >100,000 633 204 2 463 22 >100,000 1277 205 2.4 444 26 206 97 207 26 49 208 30.5 412 209 2.3 368 24 >100,000 51 260 210 11 200 40 >100,000 60 517 211 3 302 22 >100,000 7.3 212 2 70 2.5 >100,000 2.5 213 4.7 539 12 >100,000 4.2 214 4.1 436 2.5 1.1 24.5 215 2.2 270 3 0.9 16.5 216 2.8 247 4.2 >100,000 1 14.5 217 2.3 315 3.2 >100,000 1.2 218 2.8 490 0.78 >100,000 0.5 2

TABLE 4-C Comparison of Peptide Monomers and Peptide Dimers - Stability Intestinal SIF Plasma SGF Wash Cys/ (porcine) (rat) (porcine) (Rat) DTT CySS peptide Min Min Min Min Min (mV) 194 <1 5.5 195 <1 4.7 196 <4 197 198 30 4.5 199 27 81 >360 200 8 88 >360 201 18 121 >360 202 >360 >360 42 203 >293 >360 >360 21 204 >360 >360 >360 >180 27 −204 205 >360 >360 42 206 26 52 207 <20 >60 <10 35 −173 208 >360 >360 >120 <−300 209 >180 >180 >180 >180 >120 <−300 210 >300 >120 <−300 211 >300 >60 179 >120 212 90 39 98 >120 213 >180 >180 214 >810 >360 >360 >360 >120 215 >360 >360 >360 >360 >120 216 >180 >180 >360 >360 217 121 >120 >360 >180 >120 <−300 218 11 hr >360 >360 >360 >120 <−300

Example 3 Characterization of an Illustrative Peptide Dimer Molecule in Biochemical and Cell Binding Assays

Certain embodiments of the invention relate to an α4β7 integrin antagonist peptide dimer of two peptide monomer subunits each having the amino acid sequence shown below:

(SEQ ID NO: 225) Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-[Phe(4-tBu)]- (β-homoGlu)-(D-Lys).

The two peptide monomer subunits each contain an intramolecular disulfide bond between the two Pen residues present in each peptide monomer subunits.

Each of the two peptide monomer subunits contains an N-terminal acetyl group, and the two peptide monomer subunits are dimerized at each of their C-termini by the DIG linker to produce the peptide dimer referred to herein as Peptide X, which is diagrammed below:

(SEQ ID NO: 302) [Ac-Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-(Phe(4- tBu))-(β-homoGlu)-(D-Lys)]₂.

In vitro biochemical and cell binding assays were performed to further characterize Peptide X.

Biochemical and Cell Binding Assays

Biochemical competition ELISA assays were performed for α4β7 and a4(31 integrins. The ELISA assay for α4β7 is based on binding of MAdCAM-1 to immobilized α4β7, whereas the α4β1 ELISA relies on binding of soluble α4β1 to immobilized VCAM-1. These assays are described in Example 2. Under 1 mM Mg²⁺ binding conditions, the IC₅₀ for Peptide X was 3 nM and >10,000 nM for α4β7 and α4β1, respectively. In addition, the IC₅₀ for Peptide X was >100 uM for both α4β1 and αLβ2. The IC50 of Peptide X for α4β7 T cells was 1 nM.

Peptide X also blocked adhesion of MAdCAM-1 to transformed cell lines expressing α437 integrin. The Peptide X IC₅₀ for blocking adhesion of the human B cell lymphoblastoid RPMI8866 or mouse T cell TK1 cell lines to MAdCAM-1 was 0.72 nM and 0.50 nM, respectively.

Peptide X was highly selective in the cell adhesion assays. The human Jurkat cell line expresses both α4β1 and αLβ2 integrins for specific adhesion to VCAM-1 or ICAM-1, respectively. In the Jurkat/VCAM-1 or Jurkat/ICAM-1 cell adhesion assay, Peptide X was inactive at the maximum concentration tested (IC₅₀>100,000 nM). Together, these results indicated that Peptide X was specific for α4β7, and did not block the α4β1 and αLβ2 integrins.

Peptide X also blocked adhesion of memory T cells isolated from human PBMC donors. Peptide X blocked adhesion of memory T cells to MAdCAM-1. The Peptide X average IC₅₀ was 1.3 nM using cells isolated from 4 different donors. In contrast, Peptide X was inactive at the highest concentration tested in cell adhesion assays specific for α4β1 and αLβ2 (Table 5).

TABLE 5 Potency of Peptide X for memory T cells isolated from human PBMC donors. Integrin α4β7 α4β1 αLβ2 Ligand MAdCAM-1 VCAM-1 ICAM-1 IC₅₀ (nM) 1.3 >100,000 >100,000 Surface plasmon resonance (SPR) was used to further evaluate the binding properties of Peptide X. An analog of Peptide X (Peptide X-biotin), which contains a biotin group attached to Peptide X via a PEG linker, was synthesized. Another peptide dimer having the following structure, which is closely related to Peptide X, was also synthesized and biotin-labeled:

(Peptide Z) (SEQ ID NO: 67) (Ac-Pen-(N-Me-Arg)-S-D-T-L-Pen-W-E-k-NH₂)₂-DIG. Vedolizumab was also chemically biotinylated. Peptide X-biotin, Peptide Z-biotin, or biotin-labeled vedolizumab antibody was immobilized to a streptavidin coated SPR chip, and the binding of soluble α4β7 integrin was measured. The sensor grams showed that the calculated half-life for dissociation of Peptide X-biotin from α4β7 integrin was 667 min, or ˜11 hours. This half-life is quite long, and may be caused by a tight association between the peptide and the bound Mn²⁺ metal ion on the integrin. These SPR studies also showed that the KD for Peptide X-biotin was 15 nM, which was 3.8-fold lower than that for biotin-labeled vedolizumab (59 nM; Table 6). In addition, the KD for Peptide X-biotin was substantially lower than that for Peptide Z-biotin. In conclusion, these data show that the binding constants for Peptide X are superior to those for the antibody vedolizumab or a closely related peptide dimer. The K_(on)/K_(off) of Peptide X-biotin was comparable or superior to that of vedolizumab by SPR.

TABLE 6 Summary of binding rate constants for Peptide X, Peptide Z and vedolizumab. Half-life for ka kd dissociation K_(D) (M⁻¹ sec⁻¹) (sec⁻¹) (min) (nM) Peptide X-biotin 1120 0.0000173 668 15.4 Peptide Z-biotin 1048 0.0000546 211.54 52.10 Vedolizumab-biotin 4469 0.000266 43 59.5 Half-life of dissociation t_(1/2) (sec) = ln2/k_(d)

Schild analysis was used to determine if Peptide X blocked MAdCAM binding to α4β7 integrin by a simple competitive mechanism. Binding of soluble MAdCAM to immobilized α4β7 integrin protein at different Peptide X concentrations was measured by ELISA, and the results showed that antagonism was surmountable by increasing MAdCAM concentration. This result indicated that binding of Peptide X to α4β7 integrin was reversible. Based on the dose-response shifts, global-fit Schild analysis was used to determine the Schild slope and equilibrium dissociation constant (KB). The slope was ˜1, which indicated the inhibition is orthosteric antagonism with respect to MAdCAM, and not allosteric antagonism. This suggests that Peptide X and MAdCAM bind to the same site on α4β7 integrin. The estimated KB value was 1 nM, which was similar to other Peptide X potency values in different assays.

In Vitro FACS Studies

To further evaluate the selectivity of Peptide X in human blood, the fluorescent dye Alexa 647 was conjugated to Peptide X at the same position used for attaching biotin. The Peptide X Alexa 647 conjugate (Peptide X-Alexa647) was active in an RPMI8866/MAdCAM cell adhesion assay (IC₅₀=0.15 nM). Heparinized human whole blood was supplemented with 1 mM MnCl₂, and stained with the Peptide X-Alexa647 conjugate or biotinylated vedolizumab for 1 hour at room temperature. The samples were fixed (red blood cells lysed) and washed. The vedolizumab samples were stained separately with streptavidin Alexa 647 for stain for 30 minutes at room temperature. FACS analysis was used to assess binding of the peptide or vedolizumab to a broad panel of cell types including NK cells, basophils, monocytes, eosinophils, neutrophils, CD4 naïve T cells, CD4 memory T cells, CD8 naïve T cells, CD8 memory T cells, and B cells. FIG. 10 shows the binding specificities of Peptide X-Alexa647, or vedolizumab conjugated to Alexa Fluor 647, incubated with human whole blood in the presence of 1 mM MnCl₂. Table 3 shows that the binding specificities of vedolizumab and Peptide X are nearly identical in whole blood. The binding specificity for vedolizmab shown in Table 7 is also very similar to that reported in the literature (Soler et al, JPET 330:864-875, 2009).

TABLE 7 Binding specificity of vedolizumab or Peptide X-Alexa647 (1 nM) in whole blood. Percent positive staining Peptide X- Vedolizumab Alexa 647 CD4 naïve T cells 55 51 CD4 memory T cells 22 20 CD8 naïve T cells 53 52 CD8 memory T cells 36 36 CD19+ B cells 85 78 NK cells CD16+ 56+ 42 45 Basophils 86 87 Monocytes 7 7 Eosinophils 91 92 Neutrophils 0.45 0.35

Blood from cynomolgus monkeys was also analyzed by FACS. These studies showed that cells expressing α4β7 can bind vedolizumab and Peptide X simultaneously. Therefore, Peptide X binds to a site on α4β7 that is distinct from the binding site for vedolizumab.

Binding to αEβ7 integrin in cyno blood was also tested. Cyno blood was incubated with 1 nM Peptide X-Alexa647, and cells expressing α4β7 or αEβ7 were analyzed by FACS. For CD4 memory T cells, Peptide X-Alexa647 bound to α4β7⁺, but not αEβ7⁺ cells. Binding to α437 was specific, because it could be blocked in the presence of a large excess (1 uM) of unlabeled Peptide X. Therefore under these conditions, it was concluded that Peptide X binds α4β7, not αEβ7.

Example 4 In Vivo Characterization of an Illustrative Peptide Dimer Molecule

The in vivo pharmacokinetic and efficacy characteristics of Peptide X were also determined in animal studies, including pharmacokinetic studies in Cynomolgus monkeys and efficacy studies in a mouse model of DSS colitis

Pharmacokinetic Studies in Cynomolgus Monkey

To determine tissue exposure following oral administration of Peptide X, Cynomolgus monkeys were dosed with Peptide X PO QD for 8 days at 12.5 mg/kg, 25 mg/kg or 75 mg/kg. The vehicle was 50 mM phosphate buffer, pH 7. Oral bioavailability in cyno (% F) was about 0.3%. Samples were collected 4 hours after the last dose. Peptide X levels were measured by mass spectrometry and are shown in Table 8 as nM, demonstrating that Peptide X exposure was much greater in intestinal tissues compared to plasma.

TABLE 8 Peptide X exposure in cynomolgus monkey tissues Mesenteric Dose (mg/kg) Plasma Colon Small Intestine Lymph Node 12.5 2 4157 661 1501 25 5 1549 293 138 75 21 15460 7842 1980

To further evaluate the in vivo properties of Peptide X in a higher species, cynomolgus monkeys were dosed with Peptide X for 7 days. Dosing was oral (nasogastric intubation) once daily. Whole blood (about 3.5 mL) was collected on Day 0 (prior to dosing) and Day 6 (1 hour post the last dose) for PK and PD analysis. On Day 6, blood was also collected from a non-dosed animal. For PD, FACS analysis was used to measure receptor occupancy, down-regulation of α4β7 expression and circulating levels of T cells expressing the integrin α4β7. Table 9 shows the organization of the test groups.

TABLE 9 Organization of test groups for the 7 day cynomolgus monkey study Group Dose Number of animals Number Test article (mg/kg/day) Males Females 1 Peptide X 12.5 2 2 2 Peptide X 25 2 2 3 Peptide X 75 2 2

For FACS analysis, heparinized whole blood from the cynos was stained with each of two panels of antibodies to evaluate (1) the extent of α4β7 receptor occupancy in Peptide X-treated samples and (2) the abundance of circulating α4β7+, αEβ7+, and α437+αEβ7+ lymphocyte subsets. Receptor occupancy and integrin expression were assessed within memory CD4 T cells, naïve CD4 T cells, and B cells. To evaluate receptor occupancy, whole blood samples were first treated with 1 mM MnCl₂ to allow Peptide X binding, and then pre-incubated +/−1 uM unlabeled Peptide X to fully occupy (i.e., block) the α4β7 receptor. Blocked and unblocked samples were stained with 1 nM Alexa 647-labeled Peptide X, followed by staining with antibodies against α4β7, CD45, CD4, CD45RA, and CD19. Samples were processed to lyse erythrocytes and fix leukocytes, followed by staining with a second-step reagent (streptavidin-BV421) and wash steps. To assess integrin expression and cell subset abundance, whole blood samples were stained with antibodies against α4, β7, and αE, in addition to antibodies against CD45, CD4, CD45RA, and CD19. Samples were processed to lyse erythrocytes and fix leukocytes, followed by staining with a second-step reagent (streptavidin-BV421) and wash steps. All stained samples were analyzed by flow cytometry, collecting a constant sample volume to allow calculation of absolute cell counts.

FIG. 14 shows that the percent receptor occupancy in blood increases with oral dose, and that receptor occupancy exceeded 90% at the highest dose.

FIG. 15 shows the percent receptor occupancy versus Peptide X plasma concentration for each animal. By extrapolation, it was estimated that a Peptide X plasma concentration of ˜0.35 nM is sufficient to occupy 50% of the α4β7 receptors in the blood.

FIG. 16 shows that α4β7 expression on CD4 memory T cells decreased at all doses. This is consistent with binding of Peptide X inducing some internalization of α437.

Levels of circulating α4β7+ memory T cells were also measured. FIG. 17 shows that Peptide X dosing caused an increase in the percentage of α4β7+ memory T cells normalized to total CD4 cells. This is similar to the mouse studies. Blocking homing of α4β7+ memory T cells to the gut resulted in their redistribution to the blood.

Effect of Peptide X on Trafficking of a47 Memory T Cells in DSS Mice

The effect of Peptide X on memory T cell trafficking was shown in a mouse DSS colitis model. This study showed that Peptide X affects T cell homing by diverting α4β7 memory T cells from gut lymphoid tissues to the blood and spleen.

Colitis was induced in C57BL/6 male mice (10 animals per group) by exposure to 3% DSS-treated drinking water from day 0 to day 5, when animals were shifted to normal drinking water. Once daily, animal deaths were recorded, and surviving animals were weighed and assessed visually for the presence of diarrhea and/or bloody stool. Immediately prior to sacrifice on day 9, colitis severity was assessed in all animals using video endoscopy, and the resulting images were scored for colitis severity by an observer blinded to group identity.

Starting on day 0, mice were given twice-daily oral doses of either a vehicle/sham control (Group 1) or Peptide X (Group 2: 10 mg/kg, PO, BID). On day 9, only the AM treatment dose was administered. Animals in Group 2 also were administered Peptide X in their drinking water at a concentration of 0.2 mg/mL. The drinking water bottle weights for Groups 1 and 2 were measured, and water consumption was used to estimate the peptide dose ingested via the drinking water. Based on daily water consumption, the average daily Peptide X dose from the combination of oral gavage and drinking water was estimated to be 49 mg/kg.

Mice were sacrificed on day 9, approximately four hours after the final of gavage dose administration. Spleen, Peyer's patches (PP), mesenteric lymph nodes (MLN), and blood were collected from each animal and processed for FACS analysis of α4 and 37 expression on TH memory cells. Takedown and FACS analysis occurred on the same day.

These studies showed that treatment with Peptide X had no significant effect on weight loss, fluid intake, colon weight or length, or presence of bloody stool and diarrhea (data not shown). Treatment with Peptide X had a significant effect on the endoscopy scores, reducing the scores by 32% from 2.60±1.6 (vehicle) to 1.78±1.5 (Peptide X) (mean±SD; FIG. 8). Visual assessment of the endoscopy images indicated that Peptide X reduced colonic friability and improved mucosal healing compared to the vehicle control (FIG. 9).

Treatment with Peptide X had significant effects on the memory T cell populations in the blood and spleen (FIG. 10). There was a 42% increase in total α4β7 memory cells per mL blood (10A), and a 73% increase in total α437 memory cells recovered from the spleen (10B). For both blood and spleen, there also were significant increases in the number of memory cells (as a percentage of TH cells), and total memory cells. No significant difference was seen in the total number of cells in either the blood or spleen.

Treatment with Peptide X had significant effects on the α4β7+ memory T cell populations in the MLN and Peyer's patches (FIG. 11). Compared to the vehicle control, there were 23% and 55% decreases in the percentage of α4β7+ memory cells relative to total cells in the MLN (11A) and Peyer's Patches (11B), respectively.

For PK measurements, colon sections from the proximal and distal colon were collected at ˜4 hours after the last AM dose and analyzed by mass spectrometry. Exposure in the proximal colon was approximately 3-fold higher than that in the distal colon (FIG. 12). The concentration of Peptide X in the blood was 84-fold and 31-fold lower compared to that in the proximal and distal colon, respectively. Nonetheless at this time point, the plasma concentration was ˜80-fold greater than the Peptide IC₅₀ value for blocking α4β7 binding to MAdCAM.

Additional DSS colitis studies were performed, which showed that treatment with Peptide X reduced α4β7+ T cells in gut lymphoid tissues and redirected them to blood (FIG. 13). In this 9 day DSS colitis study, C57BL/6 mice were treated with 3% DSS from Day 1 to Day 6, and switched to normal water until Day 10. Daily dosing was PO BID plus drinking water for Peptide X, and 25 mg/kg IP every 3 days for the anti-α4β7 antibody DATK32. PP and blood were collected and levels of α4β7+ memory T cells analyzed by FACS.

Efficacy of Peptide Inhibitors in a Chronic DSS Colitis Mouse Model

To further evaluate the efficacy of peptides of the present invention in treating colitis, a chronic DSS colitis mouse model was used to examine the effects of orally administered Peptide X or another peptide, Peptide XX, as compared to vehicle control or the antibodies, MECA 367 and DATK32. Peptide XX is a dimer having the following structure, where DIG links the two peptide monomers by their C-termini:

(SEQ ID NO: 213) [Ac-Pen-(N-Me-Arg)-S-D-T-L-Pen-W-(β-HomoGlu)-(D- Lys)-NH₂]₂.

In this 15 day chronic DSS colitis study, BALB/c mice were treated continuously with 2.5% DSS. Peptide X dosing was 55 mg/kg/day, 17 mg/kg/day or 6 mg/kg/day in drinking water. Peptide XX dosing was 10 mg/kg PO BID plus 0.2 mg/ml in drinking water. The anti-α4β7 Ab DATK32 was dosed 25 mg/kg IP every 3 days, and the anti-MAdCAM Ab MECA 367 was dosed 8 mg/kg IP daily. After takedown, distal colon sections were fixed for histopathology and processed for β7+ cell IH staining using the anti-β7 antibody M293.

FIG. 18 shows that Peptide XX reduced colon macroscopic and histopathology scores comparable to the antibodies in a murine 15 day chronic DSS model.

FIG. 19 shows that Peptide XX reduced infiltration of B7+ cells into the lamina propria of the distal colon.

FIG. 22 shows that all doses of Peptide X reduced infiltration of B7+ cells into the lamina propria of the distal colon.

Fluorescence imaging was performed after in oral administration of vehicle or 10 mg/kg or 90 mg/kg of Peptide X conjuaged to Alexa 488 to normal C57BL6 mice (n=2 mice per group). Mice were harvested 3 hours post-dose and the following tissues were collected: 3.8 cm of proximal small intestine and 3.8 cm of distal colong. The samples were fixed in PFA and frozen in OCT, formalin-fixed, and paraffin-embedded. 5 micron slices were DAPI counter-stained to visualize nuclei and subjected to fluorescence microscopy at 40×.

Vehicle-treated animals showed no fluorescence signal in small intestine or colon. The 10 mg/kg PO treated animals showed signal in small intestine with aggregated in crpts (glandular cells). The 90 mg/kg PO treated animals showed weak signal in the epithelial lining, interstitial cells, and glandular cells, and stronger aggregates of signal in crypts and glandular cells in mucosa of the small intestine. A weak signal was present in the epithelial lining of the colon.

Small intestine samples were also examined by immunohistochemistry using an anti-Alexa 488 antibody of PFA fixed tissue. As shown in FIG. 21, Compound X staining was observed throughout the lamino propia and interstitial cells of animals treated with 10 mg/kg or 90 mg/kg of Compound X conjugated to Alexa 488.

These Examples establish that Peptide X and other peptides of the present invention are selective oral peptide antagonists of α4β7 integrin with minimal systemic exposure, and are effective in blocking T cell homing and preventing mucosal damage in murine models of IBD. Peptide X and the clinically validated anti-α4β7 antibody vedolizumab have comparable potency and selectivity in a variety of assays including cell adhesion and binding to human CD4+ memory T cells. PK studies in normal or dextran sodium sulfate (DSS) treated mice and rats show that oral dosing results in marked drug exposure in the small intestine, Peyer's Patches, colon, and mesenteric lymph nodes (MLN), but no significant measurable levels in the blood and urine. To measure the effect of oral dosing on trafficking of endogenous memory T cells, DSS mice were orally dosed daily with Peptide X for 9 days, and harvested tissues were analyzed by FACS. FACS analysis showed a dose dependent reduction of CD4⁺ CD44^(high) CD45RB^(low) (37⁺ T cells in the MLN and Peyer's Patches, and a concomitant increase in the spleen and blood. There was also a dose-dependent reduction in body weight loss and mucosal injury as assessed by endoscopy. Peptide X also showed stability to a variety of gastrointestinal (GI) fluids, metabolic enzymes and intestinal bacteria. Peptide X was shown to be an effective oral antagonist selective for α4β7 integrin. In murine colitis models, Peptide X and similar analogs blocked T cell trafficking and reduce histopathology to levels similar to that of pathway specific antibodies. In the blood of cynomolgus monkeys, Peptide X saturated blood receptor occupancy and increased circulating levels of α4β7 CD4 T cells. Peptide X's low blood exposure and high GI exposure suggests that it is locally acting within the gut lymphoid compartment to block memory T cell pathology.

All publications and patent applications described herein are hereby incorporated by reference in their entireties.

The present invention may be embodied in other specific forms without departing from its structures, methods, or other essential characteristics as broadly described herein and claimed hereinafter. The described embodiments are to be considered in all respects only as illustrative, and not restrictive. The scope of the invention is, therefore, indicated by the appended claims, rather than by the foregoing description. All changes that come within the meaning and range of equivalency of the claims are to be embraced within their scope. 

1.-41. (canceled)
 42. A method for treating Celiac disease in a subject, the method comprising administering to the subject an effective amount of a pharmaceutical composition comprising a peptide dimer compound comprising two monomer subunits, wherein each monomer subunit comprises the amino acid sequence: Pen-(N-Me-Arg)-Ser-Asp-Thr-Leu-Pen-Phe(4-tBu)-(β-homo-Glu)-(D-Lys), or a pharmaceutically acceptable salt thereof.
 43. The method of claim 42, wherein each monomer subunit comprises a disulfide bond between the two Pen amino acids.
 44. The method of claim 42, wherein the peptide dimer compound further comprises a linker moiety.
 45. The method of claim 44, wherein the linker moiety is bound to the D-Lys amino acids of the two monomer units.
 46. The method of claim 44, wherein the linker moiety is diglycolic acid (DIG).
 47. The method of claim 42, wherein the N-terminus of each monomer subunit is acylated.
 48. The method of claim 42, wherein each monomer subunit comprises a C-terminal free amide.
 49. The method of claim 42, wherein each monomer subunit comprises a disulfide bond between the two Pen amino acids and a linker moiety bound to the D-Lys amino acid, wherein the N-terminus of each monomer subunit is acylated.
 50. The method of claim 42, wherein the peptide dimer compound consists of the structure:


51. The method of claim 42, wherein the pharmaceutically acceptable salt thereof is an acetate salt of the peptide dimer compound.
 52. The method of claim 42, wherein the pharmaceutical composition is administered orally.
 53. The method of claim 42, wherein the pharmaceutical composition comprises a pharmaceutically acceptable excipient.
 54. The method of claim 42, wherein the pharmaceutical composition comprises an enteric coating.
 55. The method of claim 42, wherein the peptide dimer compound or pharmaceutically acceptable salt thereof inhibits binding of α4β7 to MAdCAM. 